TY  - JOUR

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 (GJB2) gene

JO  - Journal of Medical Genetics

PY  - 2001/01/01

AU  - Mustapha M

ED  - 

DO  - DOI: 10.1136/jmg.38.10.e36

PB  - BMJ

VL  - 38

IS  - 10

SP  - 36e

EP  - 36

Y2  - 2024/12/26

ER  -