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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

✍ Scribed by Kinoshita, K.; Miura, Y.; Nagasaki, H.; Murase, T.; Bando, Y.; Oiso, Y.

Book ID: 125336535
Publisher: Springer-Verlag
Year: 2004
Tongue: English
Weight: 88 KB
Volume: 27
Category: Article
ISSN: 0391-4097
DOI: 10.1007/BF03346263

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