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

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Departments

Item type:Organizational Unit,

School / College / Institute

Item type:Organizational Unit,
SCHOOL OF MEDICINE
Upper Org Unit

Program

Organization 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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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

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Nature Portfolio

Citation

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Source

Nature Communications

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DOI

10.1038/s41467-020-19290-y

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