A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

J CHENG; D. Y HAN; S. Z YANG; J. Y CAO; G. Y FENG; L. L DU; Y. Z ZHANG; S. Q ZHAI; W. Y YANG; X. Z LIU; L HE; H. J YUAN; P DAI; H. J SUN; R TAO; Q SUN; D YAN; W QIN; H. Y WANG; X. M OUYANG

doi:10.1111/j.1399-0004.2007.00889.x

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A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

Journal article

Peer reviewed

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family

J CHENG, D. Y HAN, S. Z YANG, J. Y CAO, G. Y FENG, L. L DU, Y. Z ZHANG, S. Q ZHAI, W. Y YANG, X. Z LIU, …

Clinical genetics, Vol.72(5), pp.471-477

2007

DOI: https://doi.org/10.1111/j.1399-0004.2007.00889.x

PMID: 17868390

Abstract

Fundamental and applied biological sciences. Psychology

Classical genetics, quantitative genetics, hybrids

Human

General aspects. Genetic counseling

Otorhinolaryngology. Stomatology

Non tumoral diseases

Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology

Medical genetics

Biological and medical sciences

Molecular and cellular biology

Genetics of eukaryotes. Biological and molecular evolution

Medical sciences

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47 Times Cited - Web of Science

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.150 Hearing Loss; 1.150.421 Cochlea
Web Of Science research areas: Genetics & Heredity
ESI research areas: Clinical Medicine

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Source: InCites

Details

Title: A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family
Creators: J CHENG - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
D. Y HAN - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
S. Z YANG - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
J. Y CAO - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
G. Y FENG - Bio-X Life Science Research Center, Shanghai Jiao Tong University, Shanghai, China
L. L DU - Department of Otolaryngology, University of Miami, Miami, FL, United States
Y. Z ZHANG - Sichuan Key Laboratory of Molecular Biology and Biotechnology, Life Science Center, Sichuan University, Chengdu, Sichuan, China
S. Q ZHAI - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
W. Y YANG - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
X. Z LIU - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
L HE - Bio-X Life Science Research Center, Shanghai Jiao Tong University, Shanghai, China
H. J YUAN - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
P DAI - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
H. J SUN - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
R TAO - Bio-X Life Science Research Center, Shanghai Jiao Tong University, Shanghai, China
Q SUN - Institute Of Otolaryngology, Chinese PLA General Hospital, Beijing, China
D YAN - Bio-X Life Science Research Center, Shanghai Jiao Tong University, Shanghai, China
W QIN - Bio-X Life Science Research Center, Shanghai Jiao Tong University, Shanghai, China
H. Y WANG - Sichuan Key Laboratory of Molecular Biology and Biotechnology, Life Science Center, Sichuan University, Chengdu, Sichuan, China
X. M OUYANG - Department of Otolaryngology, University of Miami, Miami, FL, United States
Publication Details: Clinical genetics, Vol.72(5), pp.471-477
Publisher: Blackwell; Oxford
Academic Unit: Miller School of Medicine; UMMG Department of Otolaryngology
Language: English
Resource Type: Journal article
PMID: 17868390
Record Identifier: 991031576295002976