The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation
about
A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearingStructural basis of an embryonically lethal single Ala --> Thr mutation in the vnd/NK-2 homeodomainOctamer-binding transcription factors: genomics and functions.A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families
P2860
The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation
description
1997 nî lūn-bûn
@nan
1997 թուականին հրատարակուած գիտական յօդուած
@hyw
1997 թվականին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@ast
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@en
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@nl
type
label
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@ast
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@en
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@nl
prefLabel
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@ast
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@en
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@nl
P2093
P1433
P1476
The molecular basis of X-linke ...... for a POU3F4 missense mutation
@en
P2093
C W Cremers
F P Cremers
H H Ropers
Y J de Kok
P304
P356
10.1002/(SICI)1098-1004(1997)10:3<207::AID-HUMU5>3.3.CO;2-X
P407
P577
1997-01-01T00:00:00Z