The Glycosylphosphatidylinositol biosynthesis pathway in human diseases | Orphanet Journal of Rare Diseases | Full Text

The Glycosylphosphatidylinositol biosynthesis pathway in human diseases | Orphanet Journal of Rare Diseases | Full Text

The Glycosylphosphatidylinositol biosynthesis pathway in human diseases

Glycosylphosphatidylinositol biosynthesis defects cause rare genetic disorders characterised by developmental delay/intellectual disability, seizures, dysmorphic features, and diverse congenital anomalies asso...

Authors:Tenghui Wu, Fei Yin, Shiqi Guang, Fang He, Li Yang and Jing Peng

Citation:Orphanet Journal of Rare Diseases 2020 15:129

Content type:Review

Published on: 28 May 2020

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