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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

✍ Scribed by Christensen, Jane H; Siggaard, Charlotte; Corydon, Thomas J; deSanctis, Luisa; Kovacs, Laszlo; Robertson, Gary L; Gregersen, Niels; Rittig, Søren


Book ID
110025495
Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
220 KB
Volume
12
Category
Article
ISSN
1018-4813

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