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author Rouzier, Cécile
Moore, David
Delorme, Cécile
Lacas-Gervais, Sandra
Ait-El-Mkadem, Samira
Fragaki, Konstantina
Burté, Florence
Serre, Valérie
Bannwarth, Sylvie
Chaussenot, Annabelle
Catala, Martin
Yu-Wai-Man, Patrick
Paquis-Flucklinger, Véronique
author_facet Rouzier, Cécile
Moore, David
Delorme, Cécile
Lacas-Gervais, Sandra
Ait-El-Mkadem, Samira
Fragaki, Konstantina
Burté, Florence
Serre, Valérie
Bannwarth, Sylvie
Chaussenot, Annabelle
Catala, Martin
Yu-Wai-Man, Patrick
Paquis-Flucklinger, Véronique
author_sort Rouzier, Cécile
collection PubMed
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spelling pubmed-54117372017-05-05 A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions Rouzier, Cécile Moore, David Delorme, Cécile Lacas-Gervais, Sandra Ait-El-Mkadem, Samira Fragaki, Konstantina Burté, Florence Serre, Valérie Bannwarth, Sylvie Chaussenot, Annabelle Catala, Martin Yu-Wai-Man, Patrick Paquis-Flucklinger, Véronique Hum Mol Genet Corrigenda Oxford University Press 2017-05-01 2017-04-20 /pmc/articles/PMC5411737/ /pubmed/28475771 http://dx.doi.org/10.1093/hmg/ddx130 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Corrigenda
Rouzier, Cécile
Moore, David
Delorme, Cécile
Lacas-Gervais, Sandra
Ait-El-Mkadem, Samira
Fragaki, Konstantina
Burté, Florence
Serre, Valérie
Bannwarth, Sylvie
Chaussenot, Annabelle
Catala, Martin
Yu-Wai-Man, Patrick
Paquis-Flucklinger, Véronique
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title_full A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title_fullStr A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title_full_unstemmed A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title_short A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions
title_sort novel cisd2 mutation associated with a classical wolfram syndrome phenotype alters ca(2+) homeostasis and er-mitochondria interactions
topic Corrigenda
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411737/
https://www.ncbi.nlm.nih.gov/pubmed/28475771
http://dx.doi.org/10.1093/hmg/ddx130
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