Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus [2]

Nature Genetics

Volumn 23, Issue 1, 1999, Pages 16-18

  Grifa, A ^a   A Wagner, C ^a   D'Ambrosio, L ^a   Melchionda, S ^a   Bernardi, F ^a   Lopez Bigas, N ^a   Rabionet, R ^a   Arbones, M ^a   Della Monica, M ^a   Estivill, X ^a   Zelante, L ^a   Lang, F ^a   Gasparini, P ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; CONNEXIN 30; CONNEXIN 32; GAP JUNCTION PROTEIN; THREONINE; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 13Q; GENE LOCUS; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; IN SITU HYBRIDIZATION; LETTER; MOLECULAR INTERACTION; NONHUMAN; PEDIGREE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0032846415     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/12612     Document Type: Letter

References (15)