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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vojdani, Samaneh, Jafarzadeh Esfehani, Reza, Iranmanesh, Vahid, Davari, Hafezeh, Amini, Nafiseh, Jaripour, Mohammad Ehsan, Zargari, Peyman, Dastpak, Mahtab, Sadrnabavi, Ariane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449530/
https://www.ncbi.nlm.nih.gov/pubmed/30989077

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449530/
https://www.ncbi.nlm.nih.gov/pubmed/30989077

Ejemplares similares