Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy

Neurology

Volumn 46, Issue 5, 1996, Pages 1329-1334

  Bohlega, S ^a   Tanji, K ^b   Santorelli, F M ^b   Hirano, M ^b   Al Jishi, A ^c   DiMauro, S ^b,d  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^b New York State Psychiat Inst and New York Presbyterian Hospital Columbia University Medical Center   (United States)

^c Sulaimaniah Medical Center   (Bahrain)

^d The New York Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; ASIA; AUTOSOMAL RECESSIVE DISORDER; CARDIOMYOPATHY; CONTROLLED STUDY; FEMALE; GENE DELETION; HUMAN; HUMAN CELL; MALE; MUSCLE BIOPSY; MUSCLE MITOCHONDRION; OPHTHALMOPLEGIA; PRIORITY JOURNAL;

EID: 0029996721     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.46.5.1329     Document Type: Article

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