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Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx060

Lookup NU author(s): David Moore, Florence Burté, Dr Patrick Yu Wai Man

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Abstract

© The Author 2017. Published by Oxford University Press. All rights reserved. The Authors would like to apologize for missing information in their acknowledgement. The full acknowledgement should read as follows: We thank Didier Dormant (MD, PhD) for performing the cerebral MRI of the patient and Georges Challe (MD) for the ophthalmological examination. We thank Cécile Delettre from the Institute of Neurosciences (Montpellier, France) for providing fibroblasts from the WFS1 patient. We are also grateful to Alain Lacampagne and Jeremy Fauconnier (Montpellier, France) for their help with the calcium experiments. We thank Gaëlle Augé, Bernadette Chafino and Charlotte Cochaud for technical help. This has now been corrected in the original paper and online.

Publication metadata

Author(s): Rouzier C, Moore D, Delorme C, Lacas-Gervais S, Ait-El-Mkadem S, Fragaki K, Burte F, Serre V, Bannwarth S, Chaussenot A, Catala M, Yu-Wai-Man P, Paquis-Flucklinger V

Publication type: Note

Publication status: Published

Journal: Human Molecular Genetics

Year: 2017

Volume: 26

Issue: 9

Pages: 1786-1786

Online publication date: 20/04/2017

Acceptance date: 02/04/2016

ISSN (print): 0964-6906

ISSN (electronic): 1460-2083

Publisher: Oxford University Press

URL: https://doi.org/10.1093/hmg/ddx130

DOI: 10.1093/hmg/ddx130

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