TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation
published in: American Journal of Human Genetics
date of publication: 2016-02-04
language: English
main subject: Transmembrane protein 199, glycosylation
Cites articles 31
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Article - wd:Q28116046