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A Synonymous Variant in MYO15A Enriched in the Ashkenazi Jewish Population Causes Autosomal Recessive Hearing Loss Due to Abnormal Splicing

Yoel Hirsch,Chayada Tangshewinsirikul,Kevin T. Booth,Hela Azaiez,Devorah Yefet,Adina Quint,Tzvi Weiden,Zippora Brownstein,Michal Macarov,Bella Davidov,John Pappas,Rachel Rabin,Margaret A. Kenna,Andrea M. Oza,Katherine Lafferty,Sami S. Amr,Heidi L. Rehm,Diana L. Kolbe,Kathy Frees,Carla Nishimura,Minjie Luo,Chantal Farra,Cynthia C. Morton,Sholem Y. Scher,Josef Ekstein,Karen B. Avraham,Richard J. H. Smith,Jun Shen

European Journal of Human Genetics（2021）

Cited 9|Views83
Key words
Genetic testing,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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