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Q42557586-7C89911E-1216-48D3-95D1-9411C7396CDC
Q42557586-7C89911E-1216-48D3-95D1-9411C7396CDC
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Statement
http://www.wikidata.org/entity/statement/Q42557586-7C89911E-1216-48D3-95D1-9411C7396CDC
Hereditary tyrosinemia type I: strong association with haplotype 6 in French Canadians permits simple carrier detection and prenatal diagnosis.
P2860
Q42557586-7C89911E-1216-48D3-95D1-9411C7396CDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42557586-7C89911E-1216-48D3-95D1-9411C7396CDC
rank
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type
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Statement
wasDerivedFrom
28d07aa680dcd1ddb24f2e5171a640920a6f01a5
P2860
Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient