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Q24676845-79B03F1D-F36B-457C-9F43-EAC10FBD93E0
Q24676845-79B03F1D-F36B-457C-9F43-EAC10FBD93E0
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http://www.wikidata.org/entity/statement/Q24676845-79B03F1D-F36B-457C-9F43-EAC10FBD93E0
Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)
P2860
Q24676845-79B03F1D-F36B-457C-9F43-EAC10FBD93E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676845-79B03F1D-F36B-457C-9F43-EAC10FBD93E0
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wasDerivedFrom
31e3749d287f0e878229135c98719546de00a52e
P2860
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twins.