Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial‐peroxisomal protein

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Bibliographic Details
Published inMovement disorders Vol. 32; no. 7; pp. 1108 - 1110
Main Authors Díez, H., Cortès‐Saladelafont, E., Ormazábal, A., Marmiese, A. Fernández, Armstrong, J., Matalonga, Leslie, Bravo, Miren, Briones, Paz, Emperador, Sonia, Montoya, Julio, Artuch, Rafael, Giros, Marisa, Garcia‐Cazorla, Àngels
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.07.2017
Subjects
Adult
Basal ganglia
Brain diseases
Central nervous system diseases
Fatal Outcome
Female
GTP Phosphohydrolases - genetics
Humans
Microtubule-Associated Proteins - genetics
Mitochondria
Mitochondria - metabolism
Mitochondrial Proteins - genetics
Movement disorders
Mutation
Mutation - genetics
Parkinsonian Disorders - genetics
Parkinsonian Disorders - metabolism
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Bibliography:Nothing to report.
Relevant conflicts of interests/financial disclosures
Funding agencies
This work was supported by the Plan Nacional de I+D+I and Instituto de Salud Carlos III‐ Subdirección General de Evaluación y Fomento de la Investigación Sanitaria (FIS: PI12/01951, PI14/00005) and the European Regional Development Fund (FEDER).
ISSN:0885-3185
1531-8257
DOI:10.1002/mds.27021