Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss

Journal of Genetics and Genomics

Volumn 37, Issue 12, 2010, Pages 787-793

  Li, Jianzhong ^a,b   Cheng, Jing ^a   Lu, Yanping ^a   Lu, Yu ^a   Chen, Aiting ^a   Sun, Yi ^a   Kang, Dongyang ^a   Zhang, Xin ^a   Dai, Pu ^a   Han, Dongyi ^a   Yuan, Huijun ^a  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b FUZHOU GENERAL HOSPITAL   (China)

Author keywords

DFNX2; Mutation; POU3F4; Prenatal diagnosis

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; CHINESE; FEMALE; GENE POU3F4; HUMAN; HUMAN TISSUE; MALE; MISSENSE MUTATION; MIXED HEARING LOSS; MOLECULAR MODEL; MUTATOR GENE; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PHENOTYPE; PRENATAL DIAGNOSIS; X CHROMOSOME LINKAGE;

ASIAN CONTINENTAL ANCESTRY GROUP; DNA; EAR, INNER; FEMALE; GENETIC DISEASES, X-LINKED; GLUTAMIC ACID; GLYCINE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MODELS, MOLECULAR; MUTATION, MISSENSE; PEDIGREE; POU DOMAIN FACTORS; PREGNANCY; PRENATAL DIAGNOSIS; TEMPORAL BONE; TOMOGRAPHY, X-RAY COMPUTED;

EID: 78650567577     PISSN: 16738527     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1673-8527(09)60096-5     Document Type: Article

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