Inherited Mendelian defects of nuclear-mitochondrial communication affecting the stability of mitochondrial DNA

Mitochondrion

Volumn 2, Issue 1-2, 2002, Pages 39-46

  Limongelli, Anna ^a   Tiranti, Valeria ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

Inherited Mendelian defects; Mitochondrial DNA; Nuclear mitochondrial communication

Indexed keywords

ADENINE NUCLEOTIDE TRANSLOCASE; DEOXYGUANOSINE KINASE; DEOXYRIBONUCLEOTIDE; DNA DIRECTED DNA POLYMERASE GAMMA; HELICASE; MITOCHONDRIAL DNA; THYMIDINE KINASE; THYMIDINE PHOSPHORYLASE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL INHERITANCE; AUTOSOMAL RECESSIVE DISORDER; CHILDHOOD DISEASE; CHROMOSOME 10Q; CHROMOSOME 15Q; CHROMOSOME 4Q; DNA STRAND BREAKAGE; ENCEPHALOMYOPATHY; GENE DELETION; GENE LOCUS; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HEART MUSCLE; HETEROZYGOSITY; HUMAN; INFANT DISEASE; LIVER FAILURE; MNGIE SYNDROME; MYOPATHY; OPHTHALMOPLEGIA; PATHOGENICITY; PRIORITY JOURNAL; WILD TYPE;

EID: 0036838370     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1567-7249(02)00043-0     Document Type: Review

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