Open AccessCorrection to: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
Publication year - 2022
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awac254
Subject(s) - hereditary spastic paraplegia , paraplegia , mitochondrial dna , morphology (biology) , medicine , spastic , neuroscience , anatomy , phenotype , biology , genetics , physical medicine and rehabilitation , spinal cord , gene , cerebral palsy
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