Gap Junction Protein Beta 2 Gene Variants and Non-Syndromic Hearing Impairment among Couples Referred For Prenatal Diagnosis in the Northeast of Iran

INTRODUCTION: Hearing impairment is a complex medical disorder which has genetic and non-genetic causes. Gap Junction Protein Beta 2 (GJB2) gene variant is a well-known disease-causing gene among patients with hearing impairment. The frequencies of genetic variants in the GJB2 gene are different in...

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Dades bibliogràfiques
Publicat a:Iran J Otorhinolaryngol
Autors principals: Vojdani, Samaneh, Jafarzadeh Esfehani, Reza, Iranmanesh, Vahid, Davari, Hafezeh, Amini, Nafiseh, Jaripour, Mohammad Ehsan, Zargari, Peyman, Dastpak, Mahtab, Sadrnabavi, Ariane
Format: Artigo
Idioma:Inglês
Publicat: Mashhad University of Medical Sciences 2019
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6449530/
https://ncbi.nlm.nih.gov/pubmed/30989077
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