Rare compound heterozygous missense variants in CSMD3 are associated with developmental delay, intellectual disability, and structural brain anomalies Kaisa Teele Oja,Sander Pajusalu, Anneke Kievit, Marjon van Slegtenhorst,Gina Ravenscroft,Vildan Goknur Haliloglu,Ginevra Zanni,Eugenio Maria Mercuri,Ikeoluwa A. Osei-Owusu,Anne O'Donnell-Luria,Pilvi Ilves,Katrin OunapEUROPEAN JOURNAL OF HUMAN GENETICS（2023）引用 0|浏览3暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
