A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.
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A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.Molecular and clinical studies of X-linked deafness among Pakistani families.The large Chinese family with Y-linked hearing loss revisited: clinical investigation.Frequency and specific characteristics of the incomplete partition type III anomaly in children.Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.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
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P2860
A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.
description
2006 nî lūn-bûn
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name
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@en
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@nl
type
label
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@en
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@nl
prefLabel
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@en
A novel mutation of POU3F4 cau ...... oss in a large Chinese family.
@nl
P2093
P1433
P1476
A novel mutation of POU3F4 cau ...... loss in a large Chinese family
@en
P2093
Dong-Yi Han
Qing-Zhong Li
Qiu-Ju Wang
Wei-Yan Yang
Ya-Li Zhao
P304
P356
10.1097/01.MLG.0000215285.53045.24
P407
P50
P577
2006-06-01T00:00:00Z