Open AccessCytochrome c Oxidase Deficiency Due to Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease—Correction
Author(s) -
Jae-Kyu Roh
Publication year - 2003
Publication title -
archives of neurology
Language(s) - Uncategorized
Resource type - Journals
eISSN - 1538-3687
pISSN - 0003-9942
DOI - 10.1001/archneur.60.5.749
Subject(s) - cytochrome c oxidase , philosophy , medicine , genetics , biology , mitochondrion