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An atypical Dent’s disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes

✍ Scribed by Addis, Maria; Meloni, Cristiana; Tosetto, Enrica; Ceol, Monica; Cristofaro, Rosalba; Melis, Maria Antonietta; Vercelloni, Paolo; Del Prete, Dorella; Marra, Giuseppina; Anglani, Franca


Book ID
120412239
Publisher
Nature Publishing Group
Year
2012
Tongue
English
Weight
652 KB
Volume
21
Category
Article
ISSN
1018-4813

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