Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jae Sophia Zuno"'
Autor:
Hans M Dalton, Raghuvir Viswanatha, Roderick Brathwaite, Jae Sophia Zuno, Alexys R Berman, Rebekah Rushforth, Stephanie E Mohr, Norbert Perrimon, Clement Y Chow
Publikováno v:
PLoS Genetics, Vol 18, Iss 9, p e1010430 (2022)
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://doaj.org/article/bbc74efb857641bd92e0108b5c183c6e
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