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1
Q33627507-2DC38ADD-6522-493E-A3D2-E398A10EF9CD
Q33627507-2DC38ADD-6522-493E-A3D2-E398A10EF9CD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33627507-2DC38ADD-6522-493E-A3D2-E398A10EF9CD
Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).
P2860
Q33627507-2DC38ADD-6522-493E-A3D2-E398A10EF9CD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33627507-2DC38ADD-6522-493E-A3D2-E398A10EF9CD
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ff10bdf986800f41f13df54d1963569a11021325
P2860
Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes