Analysis of theCHCHD10gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain-Reference-Cited by-同舟云学术

Analysis of theCHCHD10gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Published:2015-07-07 Issue:12 Volume:138 Page:e400-e400
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Dols-Icardo Oriol,Nebot Irene,Gorostidi Ana,Ortega-Cubero Sara,Hernández Isabel,Rojas-García Ricard,García-Redondo Alberto,Povedano Monica,Lladó Albert,Álvarez Victoria,Sánchez-Juan Pascual,Pardo Julio,Jericó Ivonne,Vázquez-Costa Juan,Sevilla Teresa,Cardona Fernando,Indakoechea Begoña,Moreno Fermín,Fernández-Torrón Roberto,Muñoz-Llahuna Laia,Moreno-Grau Sonia,Rosende-Roca Maiteé,Vela Álvaro,Muñoz-Blanco José Luís,Combarros Onofre,Coto Eliecer,Alcolea Daniel,Fortea Juan,Lleó Alberto,Sánchez-Valle Raquel,Esteban-Pérez Jesús,Ruiz Agustín,Pastor Pau,López De Munain Adolfo,Pérez-Tur Jordi,Clarimón Jordi,

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/138/12/e400/11142363/awv175.pdf

Reference10 articles.

1. An integrated map of genetic variation from 1,092 human genomes

2. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

3. Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

4. CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

5. Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

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2. Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion;Cells;2023-12-07

3. Mitochondria, a Key Target in Amyotrophic Lateral Sclerosis Pathogenesis;Genes;2023-10-24

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5. Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10–what distinguishes the two?;Frontiers in Cell and Developmental Biology;2022-09-09