Publication:
Author correction: loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

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Departments

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School / College / Institute

Organizational Unit
SCHOOL OF MEDICINE
Upper Org Unit

Program

KU Authors

Co-Authors

Elouej, Sahar
Harhouri, Karim
Mao, Morgane Le
Baujat, Genevieve
Nampoothiri, Sheela
Menabawy, Nihal Al
Selim, Laila
Paneque, Arianne Llamos
Kubisch, Christian
Lessel, Davor

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Type

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N/A

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Alternative Title

Abstract

The original version of this Article contained errors in the author affiliations. The affiliations of Nathalie Escande-Beillard and Bruno Reversade with ‘Medical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey’ were inadvertently omitted. This has now been corrected in both the PDF and HTML versions of the Article.

Source

Publisher

Nature Portfolio

Subject

Genetics , Cell biology, Medical genetics, Molecular biology

Citation

Has Part

Source

Nature Communications

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Edition

DOI

10.1038/s41467-020-19290-y

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