Adult cases of mitochondrial DNA depletion due to TK2 defect: An expanding spectrum

Neurology

Volumn 78, Issue 9, 2012, Pages 644-648

  Behin A ^a   Jardel, C ^a   Claeys, K G ^a,b   Fagart, J ^c   Louha, M ^a   Romero, N B ^a   Laforet P ^a   Eymard, B ^a   Lombes A ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^c INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; LACTIC ACID; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; CREATINE KINASE BLOOD LEVEL; DISEASE COURSE; DNA DETERMINATION; ECHOCARDIOGRAPHY; ELECTROMYOGRAM; GENE; GENE MUTATION; HUMAN; MITOCHONDRIAL MYOPATHY; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; RESPIRATORY FUNCTION; TK2 GENE;

EID: 84858270499     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e318248df2b     Document Type: Article

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