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 (<i>GJB2</i>) gene
- DOI
- 10.1136/jmg.38.10.e36
- Published
- 2001-10-01
- Container
- Journal of Medical Genetics
- Publisher
- BMJ
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1136/jmg.38.10.e36,
title = {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 (<i>GJB2</i>) gene},
author = {Myrna Mustapha and Nabiha Salem and Valérie Delague and Eliane Chouery and Michella Ghassibeh and Myriam Rai and Jacques Loiselet and Christine Petit and André Mégarbané},
year = {2001},
journal = {Journal of Medical Genetics},
doi = {10.1136/jmg.38.10.e36},
url = {https://doi.org/10.1136/jmg.38.10.e36}
}RIS
TY - JOUR TI - 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 (<i>GJB2</i>) gene AU - Myrna Mustapha AU - Nabiha Salem AU - Valérie Delague AU - Eliane Chouery AU - Michella Ghassibeh AU - Myriam Rai AU - Jacques Loiselet AU - Christine Petit AU - André Mégarbané PY - 2001 JO - Journal of Medical Genetics DO - 10.1136/jmg.38.10.e36 UR - https://doi.org/10.1136/jmg.38.10.e36 ER -
APA
Mustapha, M., Salem, N., Delague, V., Chouery, E., Ghassibeh, M., Rai, M., Loiselet, J., Petit, C., & Mégarbané, A. (2001). 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 (<i>GJB2</i>) gene. Journal of Medical Genetics. https://doi.org/10.1136/jmg.38.10.e36
Source records
- crossref · retrieved 2026-09-27T10:43:45.727Z