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Q30359286-3B6BF45C-5685-43C7-B190-F1D3E6C01E50
Q30359286-3B6BF45C-5685-43C7-B190-F1D3E6C01E50
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http://www.wikidata.org/entity/statement/Q30359286-3B6BF45C-5685-43C7-B190-F1D3E6C01E50
Wrinkled skin and fat pads in patients with ALG8-CDG: revisiting skin manifestations in congenital disorders of glycosylation.
P2860
Q30359286-3B6BF45C-5685-43C7-B190-F1D3E6C01E50
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30359286-3B6BF45C-5685-43C7-B190-F1D3E6C01E50
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wasDerivedFrom
204a29d14b1b206d9bd8507055c49a1830521058
P2860
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.