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Q43485191-6FDD0C60-D9A2-4B82-98A7-2E0E9AE2110A
Q43485191-6FDD0C60-D9A2-4B82-98A7-2E0E9AE2110A
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http://www.wikidata.org/entity/statement/Q43485191-6FDD0C60-D9A2-4B82-98A7-2E0E9AE2110A
The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.
P2860
Q43485191-6FDD0C60-D9A2-4B82-98A7-2E0E9AE2110A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43485191-6FDD0C60-D9A2-4B82-98A7-2E0E9AE2110A
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wasDerivedFrom
b7458e6375635e8dda22a7992b9e7e2214e34fbc
P2860
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.