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Q35882453-4B764EB2-6051-4487-B6BD-6A1E4D54D1A5
Q35882453-4B764EB2-6051-4487-B6BD-6A1E4D54D1A5
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http://www.wikidata.org/entity/statement/Q35882453-4B764EB2-6051-4487-B6BD-6A1E4D54D1A5
Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus
P2860
Q35882453-4B764EB2-6051-4487-B6BD-6A1E4D54D1A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35882453-4B764EB2-6051-4487-B6BD-6A1E4D54D1A5
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wasDerivedFrom
8cff57753bf97a2efa7d59e6afa3c29af955a6e4
P2860
A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency.