Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
about
Identification of a novel homozygous mutation, TMPRSS3: c.535G>A, in a Tibetan family with autosomal recessive non-syndromic hearing loss.Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE.Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment.Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.Research of genetic bases of hereditary non-syndromic hearing loss.The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.
P2860
Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@ast
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@en
type
label
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@ast
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@en
prefLabel
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@ast
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@en
P2093
P2860
P1433
P1476
Novel TMPRSS3 variants in Paki ...... -syndromic hearing impairment.
@en
P2093
P B Andrade
R L P Santos-Cortez
P2860
P356
10.1111/J.1399-0004.2011.01695.X
P577
2011-05-25T00:00:00Z