Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: Clinical, biochemical, and molecular genetic features of the 10q-linked disease

Neurology

Volumn 48, Issue 5, 1997, Pages 1244-1253

  Suomalainen, Anu ^a,b   Majander, A ^a   Wallin, M ^a   Setala K ^a   Kontula, K ^a   Leinonen, H ^a   Salmi, T ^a   Paetau, A ^a   Haltia, M ^a   Valanne, L ^a   Lonnqvist, J ^a   Peltonen, L ^a   Somer, H ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; AUTOPSY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 10Q; CHROMOSOME 3P; CLINICAL ARTICLE; EXTERNAL OPHTHALMOPLEGIA; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC LINKAGE; HUMAN; MALE; MOLECULAR GENETICS; PRIORITY JOURNAL;

EID: 0030898772     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.48.5.1244     Document Type: Article

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