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