A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

Affiliations

¹ Université Côte d'Azur, CHU, Inserm, CNRS, IRCAN, France.
² Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
³ Fédération de Neurologie, Université Pierre et Marie Curie et Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
⁴ Joint Centre for Applied Electron Microscopy, Nice Sophia-Antipolis University, Nice, France.
⁵ UMR7592 CNRS, Jacques Monod Institute, Paris Diderot University, Paris, France.
⁶ UMR 7622 CNRS et UPMC et Fédération de Neurologie, Université Pierre et Marie Curie et Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
⁷ Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
⁸ NIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.

PMID: 28475771
PMCID: PMC5411737
DOI: 10.1093/hmg/ddx130

Published Erratum

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

Cécile Rouzier et al. Hum Mol Genet. 2017.

. 2017 May 1;26(9):1786.

doi: 10.1093/hmg/ddx130.

Authors

Affiliations

¹ Université Côte d'Azur, CHU, Inserm, CNRS, IRCAN, France.
² Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
³ Fédération de Neurologie, Université Pierre et Marie Curie et Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
⁴ Joint Centre for Applied Electron Microscopy, Nice Sophia-Antipolis University, Nice, France.
⁵ UMR7592 CNRS, Jacques Monod Institute, Paris Diderot University, Paris, France.
⁶ UMR 7622 CNRS et UPMC et Fédération de Neurologie, Université Pierre et Marie Curie et Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
⁷ Department of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
⁸ NIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.

PMID: 28475771
PMCID: PMC5411737
DOI: 10.1093/hmg/ddx130

No abstract available

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Erratum for

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions.
Rouzier C, Moore D, Delorme C, Lacas-Gervais S, Ait-El-Mkadem S, Fragaki K, Burté F, Serre V, Bannwarth S, Chaussenot A, Catala M, Yu-Wai-Man P, Paquis-Flucklinger V. Rouzier C, et al. Hum Mol Genet. 2017 May 1;26(9):1599-1611. doi: 10.1093/hmg/ddx060. Hum Mol Genet. 2017. PMID: 28335035 Free PMC article.

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A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

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A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

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