Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Deafness and MYO1A[original query] |
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A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness. European journal of human genetics : EJHG 2016 Oct . Patton John, Brewer Carmen, Chien Wade, Johnston Jennifer J, Griffith Andrew J, Biesecker Leslie |
Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss. Cell journal 2018 1 20 (1): 127-131. Talebi Farah, Ghanbari Mardasi Farideh, Mohammadi Asl Javad, Tizno Saeed, Najafvand Zadeh Marzi |
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