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RT @FrontPediatrics: New Research: Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome…
RT @FrontPediatrics: New Research: Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome…
New Research: Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family: Objective: Wolcott–Rallison syndrome is a rare autosomal recessive inheritance disorder caused by the… https://t.co/