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- [23] MUTATION IN SECOND EXON OF MYO15A GENE CAUSE OF NONSYNDROMIC HEARING LOSS AND ITS ASSOCIATION IN THE ARAB POPULATION IN IRAN GENETIKA-BELGRADE, 2016, 48 (02): : 587 - 596
- [26] Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 Gene Pediatric Research, 2010, 68 : 151 - 154
- [28] A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26) JOURNAL OF MEDICAL GENETICS, 2003, 40 (12): : 879 - 884