Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?

CLINICAL GENETICS(2011)

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Clinical GeneticsVolume 80, Issue 4 p. 398-402 Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy? M Krahn, Corresponding Author M Krahn Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, France Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceMartin KrahnINSERM UMR_910, Faculté de Médecine de Marseille, 4eétage Aile Verte27 boulevard Jean Moulin, 13385 Marseille Cedex 05FranceTel.: 0033 (0)4 91 78 68 94Fax: 0033 (0)4 91 80 43 19e-mail: martin.krahn@univmed.frSearch for more papers by this authorM Goicoechea, M Goicoechea Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this authorF Hanisch, F Hanisch Neurological Department, University of Halle-Wittenberg, Germany Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorE Groen, E Groen Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorM Bartoli, M Bartoli Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceSearch for more papers by this authorC Pécheux, C Pécheux Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, FranceSearch for more papers by this authorF Garcia-Bragado, F Garcia-Bragado Servicio de Anatomía Patológica. Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorF Leturcq, F Leturcq Laboratoire de Biochimie Génétique, Hôpital Cochin, Paris, FranceSearch for more papers by this authorP-Y Jeannet, P-Y Jeannet Neuropediatric Unit, Departement of Pediatrics, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorJA Lobrinus, JA Lobrinus Institut Universitaire de Pathologie, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorS Jacquemont, S Jacquemont Service de Génétique médicale, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorJ Strober, J Strober UCSF, San Francisco, CA, USASearch for more papers by this authorJA Urtizberea, JA Urtizberea Hôpital Marin, AP-HP, Hendaye, FranceSearch for more papers by this authorA Saenz, A Saenz Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this authorK Bushby, K Bushby Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorN Lévy, N Lévy Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, France Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceSearch for more papers by this authorA Lopez de Munain, A Lopez de Munain Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this author M Krahn, Corresponding Author M Krahn Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, France Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceMartin KrahnINSERM UMR_910, Faculté de Médecine de Marseille, 4eétage Aile Verte27 boulevard Jean Moulin, 13385 Marseille Cedex 05FranceTel.: 0033 (0)4 91 78 68 94Fax: 0033 (0)4 91 80 43 19e-mail: martin.krahn@univmed.frSearch for more papers by this authorM Goicoechea, M Goicoechea Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this authorF Hanisch, F Hanisch Neurological Department, University of Halle-Wittenberg, Germany Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorE Groen, E Groen Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorM Bartoli, M Bartoli Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceSearch for more papers by this authorC Pécheux, C Pécheux Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, FranceSearch for more papers by this authorF Garcia-Bragado, F Garcia-Bragado Servicio de Anatomía Patológica. Hospital Virgen del Camino, Pamplona, SpainSearch for more papers by this authorF Leturcq, F Leturcq Laboratoire de Biochimie Génétique, Hôpital Cochin, Paris, FranceSearch for more papers by this authorP-Y Jeannet, P-Y Jeannet Neuropediatric Unit, Departement of Pediatrics, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorJA Lobrinus, JA Lobrinus Institut Universitaire de Pathologie, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorS Jacquemont, S Jacquemont Service de Génétique médicale, CHUV, Lausanne, SwitzerlandSearch for more papers by this authorJ Strober, J Strober UCSF, San Francisco, CA, USASearch for more papers by this authorJA Urtizberea, JA Urtizberea Hôpital Marin, AP-HP, Hendaye, FranceSearch for more papers by this authorA Saenz, A Saenz Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this authorK Bushby, K Bushby Institute for Human Genetics, Centre for Life, University of Newcastle, UKSearch for more papers by this authorN Lévy, N Lévy Département de Génétique Médicale, Hôpital d’Enfants de la Timone, AP-HM, Marseille, France Inserm UMR_S 910, Génétique Médicale et Génomique Fonctionnelle, Faculté de Médecine Timone, Université de la Méditerranée, Marseille, FranceSearch for more papers by this authorA Lopez de Munain, A Lopez de Munain Servicio de Neurologia and Unidad Experimental, Hospital Donostia, San Sebastian, Basque Country, SpainSearch for more papers by this author First published: 27 December 2010 https://doi.org/10.1111/j.1399-0004.2010.01620.xCitations: 14Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume80, Issue4October 2011Pages 398-402 RelatedInformation
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primary calpainopathy,eosinophilic infiltration,capn3 mutations,pathophysiological component
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