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

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

Al-Aama, JY; Al-Zahrani, HS; Jelani, M; Sabir, HS; Al-Saeedi, SA; Ahmed, S

Al-Aama, JY; Jelani, M (reprint author), King Abdulaziz Univ, Princess Al Jawhara Ctr Excellence Res Hereditary, Jeddah 21589, Saudi Arabia.

CONGENITAL ANOMALIES, 2018; 58 (1): 39

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