Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations

Neurology

Volumn 62, Issue 10, 2004, Pages 1899-1901

  Procaccio, Vincent ^a,b   Wallace, Douglas C ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CONTROLLED STUDY; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY; HUMAN; LEIGH DISEASE; MITOCHONDRIAL DNA DISORDER; NDUFS8 GENE; NUCLEOTIDE SEQUENCE; ONSET AGE; PEPTIDE ANALYSIS; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN STABILITY; SCHOOL CHILD; SYNDROME DELINEATION; WESTERN BLOTTING;

EID: 2442706495     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000125251.56131.65     Document Type: Article

References (10)

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