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Volumn 35, Issue 2, 1998, Pages 151-152
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A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)
a a a a b b c c d a |
Author keywords
Connexin 26 (GJB2); DFNB1 DFNA3; Sensorineural hearing loss
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Indexed keywords
CONNEXIN 26;
GAP JUNCTION PROTEIN;
MUTANT PROTEIN;
UNCLASSIFIED DRUG;
ARTICLE;
CHROMOSOME 13Q;
CLINICAL ARTICLE;
CONTROLLED STUDY;
ELECTROPHORESIS;
ETHNIC GROUP;
FEMALE;
GENE LOCUS;
GENE MUTATION;
GENETIC LINKAGE;
GENOTYPE;
HUMAN;
HUMAN CELL;
MALE;
MOROCCO;
PERCEPTION DEAFNESS;
POPULATION GENETICS;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
SCHOOL CHILD;
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EID: 0031982160
PISSN: 00222593
EISSN: None
Source Type: Journal
DOI: 10.1136/jmg.35.2.151 Document Type: Article |
Times cited : (30)
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References (4)
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