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

Publisher： John Wiley & Sons Inc

E-ISSN： 1741-4520|58|1|39-40

ISSN： 0914-3505

Source： CONGENITAL ANOMALIES, Vol.58, Iss.1, 2018-01, pp. : 39-40

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