Associated Papers
Ethnic variation and structure-function analysis of tauopathy-associated PERK alleles.
Park G et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes.
Abbasi F et al.
Canadian Journal of Diabetes, 2018
Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.
Behnam B et al.
Hepatitis Monthly, 2013
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