RT Journal Article
SR Electronic
T1 Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (<em>GJB2</em>) gene
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP e36
OP e36
DO 10.1136/jmg.38.10.e36
VO 38
IS 10
A1 Myrna Mustapha
A1 Nabiha Salem
A1 Valérie Delague
A1 Eliane Chouery
A1 Michella Ghassibeh
A1 Myriam Rai
A1 Jacques Loiselet
A1 Christine Petit
A1 André Mégarbané
YR 2001
UL http://jmg.bmj.com/content/38/10/e36.abstract
AB