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Ruihua Wan Selected Research

Mowat-Wilson syndrome

8/2022Identification of MMACHC and ZEB2 mutations causing coexistent cobalamin C disease and Mowat-Wilson syndrome in a 2-year-old girl.

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Ruihua Wan Research Topics

Disease

1Mowat-Wilson syndrome
08/2022
1Inborn Genetic Diseases (Disease, Hereditary)
08/2022

Drug/Important Bio-Agent (IBA)

1Vitamin B 12 (Cyanocobalamin)FDA LinkGeneric
08/2022