Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment.

Hazem KaheelAndreas BreßMohamed A HassanAftab Ali ShahMutaz Amin Mustafa Yousuf Hasan Yousuf BakhitMarlies Kniper

Published in: Genetics research international (2017)

The benefit of this study on the one hand is its first report of prelingual deafness causative gene mutations identified by sequencing technology in the Syrian families. It is obvious from the results that the deployment in biomedical research is highly effective and has a great impact on the ability to uncover the cause of genetic variation in different genetic diseases.

Keyphrases

genome wide
copy number
hearing loss
single cell
gene expression
dna methylation
genome wide identification