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Nature Genetics, ISSN 1061-4036, 07/2012, Volume 44, Issue 8, pp. 916 - 921
Journal Article
Journal Article
EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, 09/2019, Volume 27, Issue 9, pp. 1456 - 1465
Hearing impairment (HI) is characterized by extensive genetic heterogeneity. To determine the population-specific contribution of known autosomal recessive... 
GENE-MUTATIONS | ALLELES | MYO15A | CONNEXIN-26 | BIOCHEMISTRY & MOLECULAR BIOLOGY | FREQUENCY | GENETICS & HEREDITY | PHENOTYPE | POPULATIONS | DEAFNESS | SPECTRUM | GJB6 MUTATIONS | African Americans | Deafness | Population studies | Hearing impairment | Etiology | Hearing loss
Journal Article
Nature Genetics, ISSN 1061-4036, 05/2015, Volume 47, Issue 6, pp. 654 - 660
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2013, Volume 93, Issue 1, pp. 132 - 140
Journal Article
Human Mutation, ISSN 1059-7794, 10/2016, Volume 37, Issue 10, pp. 991 - 1003
ABSTRACT Deafness in humans is a common neurosensory disorder and is genetically heterogeneous. Across diverse ethnic groups, mutations of MYO15A at the DFNB3... 
micro exon | DFNB3 | myosin 15 | MYO15A | shaker 2 | deafness | giant exon | NONSYNDROMIC HEARING-LOSS |