Novel splice site mutation in EIF2AK3 gene causes Wolcott ‐Rallison syndrome in a consanguineous family from Saudi Arabia
Source: Congenital Anomalies - Category: Genetics & Stem Cells Authors: Jumana Yousuf Al ‐Aama, Hams Saeed Al‐Zahrani, Musharraf Jelani, Hesham Salih Sabir, Saad Abdullah Al‐Saeedi, Saleem Ahmed Tags: Note Source Type: research
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