Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W

Audiology and Neurotology

Volumn 12, Issue 2, 2007, Pages 77-84

  Pauw, Robert J ^a   Collin, Rob W J ^a   Huygen, Patrick L M ^a   Hoefsloot, Lies H ^a   Kremer, Hannie ^a   Cremers, Cor W R J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

DFNA9; Genotype phenotype; Sensorineural hearing impairment

Indexed keywords

COCHLIN;

ADOLESCENT; ADULT; AGE DISTRIBUTION; AGED; AREFLEXIA; ARTICLE; AUDIOLOGY; AUDIOMETRY; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY STUDY; GENE MUTATION; HEARING IMPAIRMENT; HEARING LOSS; HETEROZYGOTE; HUMAN; LONGITUDINAL STUDY; NETHERLANDS; PHENOTYPE; PHONEME; PRIORITY JOURNAL; SCHOOL CHILD; SCORING SYSTEM; VESTIBULAR DISORDER; VESTIBULAR TEST;

ADOLESCENT; ADULT; AGED; AUDIOMETRY, PURE-TONE; CHILD; DISEASE PROGRESSION; FAMILY HEALTH; FEMALE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; NETHERLANDS; PEDIGREE; PHENOTYPE; PROTEINS; REFLEX, VESTIBULO-OCULAR; SPEECH PERCEPTION;

EID: 33846786948     PISSN: 14203030     EISSN: 14219700     Source Type: Journal    
DOI: 10.1159/000097794     Document Type: Article

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