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

Autor: Addis, Maria1, Meloni, Cristiana1, Tosetto, Enrica2, Ceol, Monica2, Cristofaro, Rosalba2, Melis, Maria Antonietta1, Vercelloni, Paolo3, Del Prete, Dorella2, Marra, Giuseppina3, Anglani, Franca2
Zdroj: European Journal of Human Genetics. Jun2013, Vol. 21 Issue 6, p687-690. 4p. 1 Black and White Photograph, 1 Graph.
Databáze: Academic Search Ultimate