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Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

BACKGROUND: Wolcott–Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis. The frequency of this rare syndrome is largely unknown. OBJECTIVES: To define the frequency and spectrum of...

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Detalles Bibliográficos
Autor principal:	Habeb, Abdelhadi M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Co-Action Publishing 2013
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679509/ https://www.ncbi.nlm.nih.gov/pubmed/23759358 http://dx.doi.org/10.3402/ljm.v8i0.21137

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