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Albert Perez Marti

INSERM UMR1163, Laboratory of Epithelial Biology and Disease, Imagine Institute, Paris Descartes University, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades

Paris

France

SCHOLARLY PAPERS

1

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Scholarly Papers (1)

1.

Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A

Number of pages: 53 Posted: 17 May 2019
INSERM UMR1163, Laboratory of Epithelial Biology and Disease, Imagine Institute, Paris Descartes University, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades, INSERM UMR1163, Laboratory of Epithelial Biology and Disease, Imagine Institute, Paris Descartes University, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades, INSERM UMR1163, Laboratory of Epithelial Biology and Disease, Imagine Institute, Paris Descartes University, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades, University of Freiburg (Germany), Faculty of Medicine, Medical Center, Renal Division, University of Zurich - Institute of Anatomy, University College London - Department of Renal Medicine, University College London - Department of Renal Medicine, University of Freiburg (Germany), Faculty of Medicine, Medical Center, Renal Division and INSERM UMR1163, Laboratory of Epithelial Biology and Disease, Imagine Institute, Paris Descartes University, Sorbonne Paris Cité, Hôpital Necker-Enfants Malades
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Abstract:

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renal proximal tubules, genetic disease, nuclear hormone receptor, lipid metabolism, mitochondria, organellar stress responses