Pages that link to "Q34467485"

The following pages link to Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss (Q34467485):

Displaying 23 items.

• Autosomal recessive nonsyndromic deafness genes: a review (Q24611997) (← links)
• Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family (Q28487999) (← links)
• A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family (Q33609927) (← links)
• A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus. (Q33899295) (← links)
• High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects (Q34117173) (← links)
• Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction (Q34250259) (← links)
• Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population. (Q34681962) (← links)
• Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan (Q34689630) (← links)
• Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss (Q35839601) (← links)
• Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. (Q36349189) (← links)
• Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11 (Q36519881) (← links)
• Recessive mutations of TMC1 associated with moderate to severe hearing loss. (Q36698106) (← links)
• Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran. (Q36945804) (← links)
• Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not? (Q37206548) (← links)
• Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE. (Q37452901) (← links)
• Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations (Q37782545) (← links)
• Emerging Gene Therapies for Genetic Hearing Loss (Q40080564) (← links)
• Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India (Q47142967) (← links)
• Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing (Q50353775) (← links)
• Identification of four TMC1 variations in different Chinese families with hereditary hearing loss. (Q52588849) (← links)
• Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China. (Q52658256) (← links)
• Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss. (Q53727447) (← links)
• Distinct functions of TMC channels: a comparative overview (Q90477574) (← links)