Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Maryam SobhaniMohammad Amin TabatabaiefarSeyedeh Morvarid NeishabouriAsadollah RajabSarah MozafarpourSamaneh NasrniyaAbdol-Mohammad KajbafzadehMohammad Reza Noori-Daloii

Published in: Endocrine (2019)

The current study adds to the mutation repository of WS and shows a panel of mutations in Iranian population. Such panel would facilitate genetic counseling and prenatal diagnosis in families with WS cases.

Keyphrases

genome wide
gene expression
smoking cessation
dna methylation
copy number
hiv testing
men who have sex with men