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Open Access
Peer-reviewed
Research Article
Lack of GDAP1 Induces Neuronal Calcium and Mitochondrial Defects in a Knockout Mouse Model of Charcot-Marie-Tooth Neuropathy
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Manuela Barneo-Muñoz ,
Contributed equally to this work with: Manuela Barneo-Muñoz, Paula Juárez
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain
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Paula Juárez ,
Contributed equally to this work with: Manuela Barneo-Muñoz, Paula Juárez
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain
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Azahara Civera-Tregón,
Affiliation Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain
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Laura Yndriago,
Affiliation Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain
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David Pla-Martin,
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain
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Jennifer Zenker,
Affiliation Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
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Carmen Cuevas-Martín,
Affiliations CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain, Centro de Biología Molecular Severo Ochoa, UAM-CSIC, Madrid, Spain, Instituto de Investigación Hospital 12 de Octubre, Universidad Autónoma de Madrid, Madrid, Spain
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Anna Estela,
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain
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María Sánchez-Aragó,
Affiliations CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain, Centro de Biología Molecular Severo Ochoa, UAM-CSIC, Madrid, Spain, Instituto de Investigación Hospital 12 de Octubre, Universidad Autónoma de Madrid, Madrid, Spain
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Jerónimo Forteza-Vila,
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, Instituto Valenciano de Patología, Catholic University of Valencia, Valencia, Spain
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José M. Cuezva,
Affiliations CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain, Centro de Biología Molecular Severo Ochoa, UAM-CSIC, Madrid, Spain, Instituto de Investigación Hospital 12 de Octubre, Universidad Autónoma de Madrid, Madrid, Spain
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Roman Chrast,
Affiliations Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland, Department of Neuroscience and Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
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Francesc Palau
* E-mail: fpalau@cipf.es
Affiliations Program in Rare and Genetic Diseases and IBV/CSIC Associated Unit, Centro de Investigación Príncipe Felipe, Valencia, Spain, CIBER de Enfermedades Raras (CIBERER), ISCIII, Valencia and Madrid, Spain, University of Castilla-La Mancha School of Medicine at Ciudad Real, Ciudad Real, Spain
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Lack of GDAP1 Induces Neuronal Calcium and Mitochondrial Defects in a Knockout Mouse Model of Charcot-Marie-Tooth Neuropathy
- Manuela Barneo-Muñoz,
- Paula Juárez,
- Azahara Civera-Tregón,
- Laura Yndriago,
- David Pla-Martin,
- Jennifer Zenker,
- Carmen Cuevas-Martín,
- Anna Estela,
- María Sánchez-Aragó,
- Jerónimo Forteza-Vila
- Published: April 10, 2015
- https://doi.org/10.1371/journal.pgen.1005115