Associated Papers
Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.
Aldrian D et al.
Liver International : Official Journal of the International Association for the Study of the Liver, 2024
38230874 (PubMed )
Supplement: supplement_1.pdf
Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature.
Ozbek MN et al.
Pediatric Diabetes, 2010
Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome.
Søvik O et al.
Journal of Inherited Metabolic Disease, 2008
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