Wolcott-Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene. Gaur BK, Varshney C, Rawat A, Jain S, et al. J Pediatr Endocrinol Metab 2025;39:102-105.

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Amedeo Smart

Independent Medical Education

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Gaur BK, Varshney C, Rawat A, Jain S, et al. Wolcott-Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene. J Pediatr Endocrinol Metab 2025;39:102-105.
PMID: 40990967