Autosomal dominant nonsyndromic hearing impairment

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 89, Issue 3, 1999, Pages 167-174

  Van Laer, Lut ^b   Mcguirt, Wyman T ^b   Yang, Tao ^b   Smith, Richard J H ^b   Van Camp, Guy ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b NONE

Author keywords

Autosomal dominant; Gene identification; Hearing loss

Indexed keywords

GAP JUNCTION PROTEIN; MYOSIN;

AUTOSOMAL DOMINANT DISORDER; COCHLEA DUCT; GENE LOCUS; GENE MAPPING; HEARING IMPAIRMENT; HEARING LOSS; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; REVIEW;

DEAFNESS; GENES, DOMINANT; HUMANS; MUTATION;

EID: 0033600945     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990924)89:3<167::AID-AJMG7>3.0.CO;2-V     Document Type: Review

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