Autosomal recessive nonsyndromic hearing loss

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 89, Issue 3, 1999, Pages 123-129

  Sundstrom, Rachel A ^b   Van Laer, Lut ^b   Van Camp, Guy ^b   Smith, Richard J H ^a  

^a UNIVERSITY OF IOWA   (United States)

^b NONE

Author keywords

GJB2; MYO15; MYO7A; OTOF; PDS; TECTA

Indexed keywords

CONNEXIN 26; GAP JUNCTION PROTEIN; MYOSIN;

AUTOSOMAL RECESSIVE DISORDER; COCHLEA DUCT; CONSANGUINEOUS MARRIAGE; GENE LOCATION; HEARING IMPAIRMENT; HEARING LOSS; PHENOTYPE; PRIORITY JOURNAL; REVIEW;

DEAFNESS; GENES, RECESSIVE; GENETIC DISEASES, INBORN; HUMANS; MYOSINS;

EID: 0033600947     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990924)89:3<123::AID-AJMG2>3.0.CO;2-P     Document Type: Review

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