The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study - Détails de la publication

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The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study

Auteur

Moussaoui Abdelmajid ,MeriemEl Qabli, Latifa Adarmouch, Nisrine Aboussair

Revue

Meta Gene

Année

2021

DOI

doi.org/10.1016/j.mgene.2021.100895

Chercheur

ABOUSSAIR NISRINE

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