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Q46035650-C210B233-4674-4AA8-991F-A389BCC54B61
Q46035650-C210B233-4674-4AA8-991F-A389BCC54B61
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46035650-C210B233-4674-4AA8-991F-A389BCC54B61
Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency.
P2860
Q46035650-C210B233-4674-4AA8-991F-A389BCC54B61
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46035650-C210B233-4674-4AA8-991F-A389BCC54B61
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4a9c13e281243211b5700c4adfc71feae02eeb0b
P2860
Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome.