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Q44885653-59CBB50F-C8DE-4CD1-A162-04FA8A23FC96
Q44885653-59CBB50F-C8DE-4CD1-A162-04FA8A23FC96
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Statement
http://www.wikidata.org/entity/statement/Q44885653-59CBB50F-C8DE-4CD1-A162-04FA8A23FC96
A novel deletion mutation in the arginine vasopressin receptor 2 gene and skewed X chromosome inactivation in a female patient with congenital nephrogenic diabetes insipidus.
P2860
Q44885653-59CBB50F-C8DE-4CD1-A162-04FA8A23FC96
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-59CBB50F-C8DE-4CD1-A162-04FA8A23FC96
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type
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wasDerivedFrom
be12c62cafd7af6e28c1791738749a16c8cd1095
P2860
Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.