☆ 4.0 Article

Novel splice site mutation in EIF2AK3 gene causes Wolcott-Rallison syndrome in a consanguineous family from Saudi Arabia

CONGENITAL ANOMALIES (2018)

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Journal

CONGENITAL ANOMALIES
Volume 58, Issue 1, Pages 39-40

Publisher

WILEY
DOI: 10.1111/cga.12217

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Pediatrics

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  1. King Abdulaziz City for Science and Technology [T-1382166]

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