Wolcott–Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene
Year: 2025
Type: article
Study design: Case Report
Authors: Bablu Kumar Gaur, Chirag Varshney, Aditi Rawat, Shruti Jain
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4414474726