A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
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Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing lossRNA Interference Prevents Autosomal-Dominant Hearing Loss.Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.Identification of Pathogenic Genes of Nonsyndromic Hearing Loss in Uyghur Families Using Massively Parallel DNA Sequencing Technique.Identification of four TMC1 variations in different Chinese families with hereditary hearing loss.Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.Structural relationship between the putative hair cell mechanotransduction channel TMC1 and TMEM16 proteins
P2860
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P2860
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
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2015 nî lūn-bûn
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name
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
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type
label
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
@en
prefLabel
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
@en
P2093
P1433
P1476
A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family
@en
P2093
Abdelhamid Barakat
Amina Bakhchane
Halima Nahili
Hassan Rouba
Majida Charif
Rachida Roky
P356
10.1016/J.GENE.2015.07.075
P407
P577
2015-07-28T00:00:00Z