Screening of SLC26A4 (PDS) gene mutation in cochlear implant recipients with inner ear malformation

National Medical Journal of China

Volumn 87, Issue 40, 2007, Pages 2820-2824

  Chen, Dong Ye ^a   Chen, Xiao Wei ^a   Jin, Xin ^a   Zuo, Jin ^a   Wei, Chao Gang ^a   Cao, Ke Li ^a   Fang, Fu De ^a  

^a PEKING UNION MEDICAL COLLEGE HOSPITAL   (China)

Author keywords

Acquired; Cochlear implantation; Ear deformities; Mutation; Vestibular aqueduct

Indexed keywords

ADENOSINE; GENE PRODUCT; GENOMIC DNA; GUANINE; PROTEIN SLC26A4; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; BLOOD SAMPLING; BONE MALFORMATION; CHILD; CLINICAL ARTICLE; COCHLEA PROSTHESIS; COCHLEAR NERVE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; CORRELATION ANALYSIS; DNA EXTRACTION; ELECTROSTIMULATION; EVOKED AUDITORY RESPONSE; EXON; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; INNER EAR MALFORMATION; INTRON; MALE; NERVE POTENTIAL; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEIC ACID BASE SUBSTITUTION; PEROPERATIVE CARE; POLYMERASE CHAIN REACTION; PREVALENCE; RECIPIENT; SEQUENCE ANALYSIS; TELEMETRY; TEMPORAL BONE; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; ANION TRANSPORT PROTEINS; CHILD; CHILD, PRESCHOOL; CHINA; COCHLEAR IMPLANTATION; EAR, INNER; EXONS; FEMALE; GENE FREQUENCY; GENETIC SCREENING; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; PREVALENCE; VESTIBULAR AQUEDUCT;

EID: 38549127703     PISSN: 03762491     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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