Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.
about
A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencingFrequency and specific characteristics of the incomplete partition type III anomaly in children.A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.
P2860
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P2860
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@ast
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@en
type
label
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@ast
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@en
prefLabel
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@ast
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@en
P2093
P2860
P50
P356
P1433
P1476
Cytoplasmic mislocalization of ...... o deafness in humans and mice.
@en
P2093
Birgit Rathkolb
Danielle R Lenz
Daphne Karfunkel
Kathy Ushakov
Manuela Mohr
Michael Wolf
Moshe Frydman
Shaked Shivatzki
Sibylle Sabrautzki
Yisgav Shapira
P2860
P304
P356
10.1002/HUMU.22339
P577
2013-05-08T00:00:00Z