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Expression of three different mutations in the arginine vasopressin gene suggests genotype–phenotype correlation in familial neurohypophyseal diabetes insipidus kindreds : (Genotype–phenotype correlation in familial neurohypophyseal diabetes insipidus)

✍ Scribed by Charlotte Siggaard; Jane H. Christensen; Thomas J. Corydon; Søren Rittig; Gary L. Robertson; Niels Gregersen; Lars Bolund; Erling B. Pedersen

Book ID: 108703229
Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 390 KB
Volume: 63
Category: Article
ISSN: 0300-0664
DOI: 10.1111/j.1365-2265.2005.02327.x

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Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis

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