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Autor:
Hans M. Dalton, Raghuvir Viswanatha, Ricky Brathwaite, Jae Sophia Zuno, Stephanie E. Mohr, Norbert Perrimon, Clement Y. Chow
Partial loss-of-function mutations in glycosylation pathways underlie a set of rare diseases called Congenital Disorders of Glycosylation (CDGs). In particular, DPAGT1-CDG is caused by mutations in the gene encoding the first step in N-glycosylation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13641d53275671d6ceff72f6a3c66ca6
https://doi.org/10.1101/2021.12.03.471178
https://doi.org/10.1101/2021.12.03.471178
