DFNB9 and DFNB12
Adv Otorhinolaryngol
.
2000:56:164-7.
doi: 10.1159/000059097.
Authors
S Yasunaga
1
,
M Grati
,
C Petit
Affiliation
1
Unité de Génétique des Déficits Sensoriels, Institut Pasteur, Paris, France.
PMID:
10868229
DOI:
10.1159/000059097
No abstract available
Publication types
Review
MeSH terms
Chromosome Mapping
Chromosomes, Human, Pair 10*
Chromosomes, Human, Pair 2*
Consanguinity
Deafness / genetics*
Hearing Loss, Sensorineural / genetics*
Humans