Mitochondrial encephalomyopathies

Journal article

Peer reviewed

S DiMauro, M Zeviani, C T Moraes, H Nakase, R Rizzuto, A Lombes, S Shanske and E A Schon

Progress in clinical and biological research, Vol.306, pp.117-128

1989

PMID: 2544896

Abstract

Chromosome Deletion

Central Nervous System Diseases - genetics

Central Nervous System Diseases - pathology

Optic Atrophies, Hereditary - genetics

Mitochondria, Muscle - pathology

Humans

Mitochondria, Muscle - metabolism

Male

Optic Atrophies, Hereditary - pathology

Electron Transport Complex IV - genetics

Leigh Disease - genetics

Neuromuscular Diseases - metabolism

Neuromuscular Diseases - pathology

Central Nervous System Diseases - metabolism

Neuromuscular Diseases - genetics

Syndrome

Female

Cytochrome-c Oxidase Deficiency

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Title: Mitochondrial encephalomyopathies
Creators: S DiMauro - Department of Neurology, Columbia-Presbyterian Medical Center, New York, NY 10032
M Zeviani
C T Moraes
H Nakase
R Rizzuto
A Lombes
S Shanske
E A Schon
Publication Details: Progress in clinical and biological research, Vol.306, pp.117-128
Publisher: United States
Grant note: NS 11766 / NINDS NIH HHS
Academic Unit: Miller School of Medicine; UMMG Department of Neurology
Language: English
Resource Type: Journal article
PMID: 2544896
Record Identifier: 991031559318002976