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Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial‐peroxisomal protein
Author(s) -
Díez H.,
CortèsSaladelafont E.,
Ormazábal A.,
Marmiese A. Fernández,
Armstrong J.,
Matalonga Leslie,
Bravo Miren,
Briones Paz,
Emperador Sonia,
Montoya Julio,
Artuch Rafael,
Giros Marisa,
GarciaCazorla Àngels
Publication year - 2017
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.27021
Subject(s) - peroxisome , parkinsonism , mutation , web site , mitochondrion , mitochondrial dna , computational biology , world wide web , genetics , biology , computer science , information retrieval , the internet , medicine , gene , disease
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