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ReviewCells2022

NGLY1 Deficiency, a Congenital Disorder of Deglycosylation: From Disease Gene Function to Pathophysiology.

Ashutosh Pandey et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

23 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 35406718