Disorders of nuclear-mitochondrial intergenomic signalling

Journal of Bioenergetics and Biomembranes

Volumn 29, Issue 2, 1997, Pages 121-130

  Zeviani, Massimo ^a,b   Petruzzella, Vittoria ^a   Carrozzo, Rosalba ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Maternal inheritance; Mitochondrial disorders; Mitochondrial replication; mtDNA; mtDNA depletion; Multiple mtDNA deletions; Oxidative phosphorylation; PEO; Respiratory chain

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENCEPHALOMYOPATHY; EXTERNAL OPHTHALMOPLEGIA; EXTRACHROMOSOMAL INHERITANCE; GENE DELETION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; OXIDATIVE PHOSPHORYLATION; RESPIRATORY CHAIN;

CELL NUCLEUS; DNA, MITOCHONDRIAL; GENE DELETION; GENETIC DISEASES, INBORN; HUMANS; MITOCHONDRIA; MITOCHONDRIAL ENCEPHALOMYOPATHIES; PEDIGREE; SIGNAL TRANSDUCTION; SYNDROME;

EID: 0030837619     PISSN: 0145479X     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1022633912917     Document Type: Article

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