Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

Journal: Nature Communications

Published: 2020-09-11

DOI: 10.1038/s41467-020-18146-9

Affiliations: 22

Authors: 30

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Institutions Share
Marseille Medical Genetics Center (MMG), France 0.16
CeleScreen SAS, France 0.08
University Medical Center Hamburg-Eppendorf (UKE), UHH, Germany 0.07
Institute of Medical Biology (IMB), A*STAR, Singapore 0.07
Centogene AG, Germany 0.07
MITOVASC, France 0.07
Hebrew University of Jerusalem (HUJI), Israel 0.07
Cairo University (CU), Egypt 0.07
Koç University (KU), Turkey 0.07
Hôpital Necker-Enfants Malades, France 0.05
Imagine Institute, France 0.05
Hospital Timone, France 0.04
Hospital de Especialidades Fuerzas Armadas No.1 (Hospital FF AA No.1), Ecuador 0.03
Amrita Vishwa Vidyapeetham (Amrita University), India 0.03
Institute of Myology, France 0.03
CEA Fundamental Research Division (DRF), France 0.02
Fondation Jean Dausset - CEPH, France 0.02
Hôpital Lariboisière, France 0.01
NeuroDiderot, France 0.01

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