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Q24338530-384BC834-EED3-4E59-8058-BA9781E48838
Q24338530-384BC834-EED3-4E59-8058-BA9781E48838
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338530-384BC834-EED3-4E59-8058-BA9781E48838
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
P2860
Q24338530-384BC834-EED3-4E59-8058-BA9781E48838
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24338530-384BC834-EED3-4E59-8058-BA9781E48838
rank
NormalRank
type
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Statement
wasDerivedFrom
bd28525cb21572597e579b9e360c1574b6f50244
P2860
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.