Characterization of the mitochondrial genome in childhood multiple sclerosis. III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes

Neuropediatrics

Volumn 29, Issue 6, 1998, Pages 313-319

  Ohlenbusch, A ^a   Wilichowski, E ^a   Hanefeld, F ^a  

^a UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

Author keywords

Genetic susceptibility; Mitochondrial DNA mutations; Multiple sclerosis

Indexed keywords

ADENOSINE TRIPHOSPHATASE; MITOCHONDRIAL DNA; RIBOSOME RNA; TRANSFER RNA;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENE MUTATION; GENETIC CONSERVATION; GENETIC SUSCEPTIBILITY; HUMAN; MALE; MISSENSE MUTATION; MULTIPLE SCLEROSIS; NUCLEOTIDE SEQUENCE; OPTIC NERVE DISEASE; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0032412302     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973584     Document Type: Article

References (8)

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