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Q44885653-36D9A621-9F12-460E-9069-2D8843CAF714
Q44885653-36D9A621-9F12-460E-9069-2D8843CAF714
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-36D9A621-9F12-460E-9069-2D8843CAF714
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.
P1433
Q44885653-36D9A621-9F12-460E-9069-2D8843CAF714
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-36D9A621-9F12-460E-9069-2D8843CAF714
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a48fcc00322041eaee2e3bb38fcff85de0020490
P1433
Journal of Endocrinological Investigation