The expanding spectrum of nuclear gene mutations in mitochondrial disorders

Seminars in Cell and Developmental Biology

Volumn 12, Issue 6, 2001, Pages 407-416

  Zeviani, Massimo ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Mitochondria; Mutation; Nuclear DNA; Oxidative phosphorylation; Respiratory chain

Indexed keywords

FRATAXIN; IRON BINDING PROTEIN; IRON COMPLEX; METALLOPROTEINASE; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN; UBIDECARENONE;

ATAXIA; BIOGENESIS; CEREBRAL BLINDNESS; CLINICAL FEATURE; DEGENERATIVE DISEASE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSPHAGIA; DYSTONIA; FRIEDREICH ATAXIA; GENE; GENE ABC7; GENE BCS1; GENE COX; GENE DDP1; GENE MUTATION; GENE SCO1; GENE SCO2; GENE SURF 1; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; IRON METABOLISM; MITOCHONDRION; MOHR TRANEBJAERG SYNDROME; NONHUMAN; OPTIC NERVE ATROPHY; OXIDATIVE PHOSPHORYLATION; PARANOIA; PARAPLEGIA; PERCEPTION DEAFNESS; PROTEIN TRANSPORT; RESPIRATORY CHAIN; REVIEW; SIDEROBLASTIC ANEMIA; YEAST;

EID: 0035782927     PISSN: 10849521     EISSN: None     Source Type: Journal    
DOI: 10.1006/scdb.2001.0278     Document Type: Article

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