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Q34093285-5F417F0C-BFC3-42A3-9118-444C2118ECC1
Q34093285-5F417F0C-BFC3-42A3-9118-444C2118ECC1
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Statement
http://www.wikidata.org/entity/statement/Q34093285-5F417F0C-BFC3-42A3-9118-444C2118ECC1
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.
P2860
Q34093285-5F417F0C-BFC3-42A3-9118-444C2118ECC1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34093285-5F417F0C-BFC3-42A3-9118-444C2118ECC1
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wasDerivedFrom
1c008aaeca63e22dfc4b34aa5f64b4251ff66864
P2860
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies