about
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossA de novo deletion mutation in SOX10 in a Chinese family with Waardenburg syndrome type 4.Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations.Unilateral Sensorineural Hearing Loss: Medical Context and Etiology.Efficient Generation of Gene-Modified Pigs Harboring Precise Orthologous Human Mutation via CRISPR/Cas9-Induced Homology-Directed Repair in Zygotes.The outcome of cochlear implantation among children with genetic syndromes.
P2860
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
SOX10 mutations mimic isolated hearing loss.
@en
SOX10 mutations mimic isolated hearing loss.
@nl
type
label
SOX10 mutations mimic isolated hearing loss.
@en
SOX10 mutations mimic isolated hearing loss.
@nl
prefLabel
SOX10 mutations mimic isolated hearing loss.
@en
SOX10 mutations mimic isolated hearing loss.
@nl
P2093
P2860
P50
P356
P1433
P1476
SOX10 mutations mimic isolated hearing loss.
@en
P2093
F Denoyelle
H Ducou Le Pointe
N Noël-Pétroff
V Couloigner
P2860
P304
P356
10.1111/CGE.12506
P577
2014-09-25T00:00:00Z