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See Latest ArticlesPhenotypic heterogenity of TCF2's gene mutation coding for HNF-1beta in a single family
Néphrologie & Thérapeutique , 07/28/09
Rigothier C et al. – The coexistence in the same family of pleiomorphic renal malformations (cysts, renal agenesia or hypoplasia, renal failure) with Mody–type diabetes, with an autosomal inheritance must lead to the search for a mutation of TCF2, one of the most frequent genetic renal diseases.
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Paracrine/endocrine mechanism of stem cells on kidney repair: role of microvesicle-mediated transfer of genetic information
Current Opinion in Nephrology and Hypertension, 12/17/09
Susceptibility genes in common complex kidney disease
Current Opinion in Nephrology and Hypertension, 12/17/09
The Changing Phenotype of Academic Nephrology— A Future at Risk
Clinical Journal of the American Society of Nephrology, 12/15/09
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