Disease: Deafness- autosomal dominant nonsyndromic sensorineural 24
- <em>MCM2</em> mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family
- <em>TBC1D24</em>-Related Disorders
- A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3
- A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter
- Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss
- Evaluation of deaf children in a large series in Turkey
- Genetics of congenital deafness
- MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family
- MYH9: Structure, functions and role of non-muscle myosin IIA in human disease
- POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
- The relationship between the GJB3 c.538C>T variant and hearing phenotype in the Chinese population
- Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss