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Q44885653-C62A121E-5BB6-4A8E-ADA0-641C2F88C339
Q44885653-C62A121E-5BB6-4A8E-ADA0-641C2F88C339
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Statement
http://www.wikidata.org/entity/statement/Q44885653-C62A121E-5BB6-4A8E-ADA0-641C2F88C339
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-C62A121E-5BB6-4A8E-ADA0-641C2F88C339
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44885653-C62A121E-5BB6-4A8E-ADA0-641C2F88C339
rank
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type
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wasDerivedFrom
be12c62cafd7af6e28c1791738749a16c8cd1095
P2860
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutation.