Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

Annals of Neurology

Volumn 49, Issue 5, 2001, Pages 607-617

  Barthélémy, Cyrille ^a   De Baulny, Hélène Ogier ^b   Diaz, Jorge ^c   Cheval, Marie Armelle ^d   Frachon, Paule ^a   Romero, Norma ^a   Goutieres, Françoise ^e   Fardeau, Michel ^a   Lombès, Anne ^a  

^a INSERM   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

^c Faculte de Pharmacie   (France)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CYTOCHROME C OXIDASE; LACTIC ACID; MITOCHONDRIAL DNA; PROTEIN; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ADOLESCENT; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FEMALE; HUMAN; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; KEARNS SAYRE SYNDROME; MALE; MUSCLE BIOPSY; MYOPATHY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

AGE OF ONSET; BLOTTING, SOUTHERN; CHILD; DNA, MITOCHONDRIAL; DOSAGE COMPENSATION, GENETIC; FEMALE; GENE DELETION; GENE DOSAGE; HUMANS; IN SITU HYBRIDIZATION; KEARNS-SAYER SYNDROME; MALE; MUSCLES;

EID: 0342502189     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1002     Document Type: Article

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