Variants of OTOF and PJVK genes in Chinese patients with auditory neuropathy spectrum disorder

PLoS ONE

Volumn 6, Issue 9, 2011, Pages

  Wang, Jian ^a   Fan, Ying Ying ^b   Wang, Shu juan ^a   Liang, Penf Fei ^a   Wang, Jin Ling ^a   Qiu, Jian Hua ^a  

^a FOURTH MILITARY MEDICAL UNIVERSITY   (China)

^b FOURTH MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUDITORY NEUROPATHY SPECTRUM DISORDER; CHILD; CHINESE; CONTROLLED STUDY; EXON; FEMALE; GENE; GENE SEQUENCE; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OTOF GENE; PJVK GENE; PRESCHOOL CHILD; SCHOOL CHILD; VESTIBULOCOCHLEAR NERVE DISEASE;

ADOLESCENT; ADULT; AGE OF ONSET; AMINO ACID SEQUENCE; CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; HEARING LOSS, CENTRAL; HETEROZYGOTE; HUMANS; MALE; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; NERVE TISSUE PROTEINS; PHENOTYPE; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 80052854637     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0024000     Document Type: Article

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