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Paper Details

Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.
Hum Mutat
14
2019
Author NameAffiliation
Daniel C KoboldtInstitute for Genomic Medicine, Nationwide Children's Hospital
Daniel C KoboldtThe Ohio State University
Richard K WilsonInstitute for Genomic Medicine, Nationwide Children's Hospital
Richard K WilsonNationwide Children's Hospital
Richard K WilsonInstitute for Genomic Medicine, Nationwide Children's Hospital
Richard K WilsonNationwide Children's Hospital
Kandamurugu ManickamThe Ohio State University
Kandamurugu ManickamNationwide Children's Hospital
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Datasets

Release 1.2