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 |
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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 |
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