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Q24315130-D4A7B643-E90E-4A70-99C7-A71383509F31
Q24315130-D4A7B643-E90E-4A70-99C7-A71383509F31
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http://www.wikidata.org/entity/statement/Q24315130-D4A7B643-E90E-4A70-99C7-A71383509F31
Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism
P2860
Q24315130-D4A7B643-E90E-4A70-99C7-A71383509F31
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24315130-D4A7B643-E90E-4A70-99C7-A71383509F31
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wasDerivedFrom
929a098a5f3cbd9ca904f11cfc1e15e966c78fcc
P2860
A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency.