Cracking the auditory genetic code: Nonsyndromic hereditary hearing impairment

American Journal of Otology

Volumn 20, Issue 1, 1999, Pages 115-132

  Lalwani, Anil K ^a   Castelein, Caley M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; DYSTROPHIN; MYOSIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC CODE; HEARING IMPAIRMENT; HUMAN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

CHROMOSOME MAPPING; GENE FREQUENCY; GENES, RECESSIVE; HEARING DISORDERS; HUMANS; MOLECULAR BIOLOGY; PEDIGREE; PHENOTYPE;

EID: 0032935303     PISSN: 01929763     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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