Depletion of the other genome-mitochondrial DNA depletion syndromes in humans

Journal of Molecular Medicine

Volumn 80, Issue 7, 2002, Pages 389-396

  Elpeleg, Orly ^a,b   Mandel, Hanna ^c   Saada, Ann ^a  

^a SHAARE ZEDEK MEDICAL CENTER   (Israel)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^c TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

DNA replication; Mitochondrial DNA; mtDNA depletion; Multiple deletions

Indexed keywords

ADENINE NUCLEOTIDE TRANSLOCASE; CARRIER PROTEIN; DEOXYGUANOSINE KINASE; DEOXYRIBONUCLEOSIDE; DEOXYRIBONUCLEOTIDE; DNA POLYMERASE; GENOMIC DNA; HELICASE; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; NUCLEOTIDE; PHOSPHOTRANSFERASE; STRUCTURAL PROTEIN; THYMIDINE KINASE; THYMIDINE PHOSPHORYLASE; THYMIDINE KINASE 2;

BRAIN DISEASE; CLINICAL FEATURE; DISEASE COURSE; DNA REPLICATION; DNA SEQUENCE; ENZYME ACTIVITY; ENZYME DEFICIENCY; EXERCISE TOLERANCE; FATALITY; GENE DELETION; GENE FUNCTION; GENE IDENTIFICATION; GENE MUTATION; GENE POOL; GENETIC CODE; HUMAN; INFANCY; KIDNEY TUBULE DISORDER; LINKAGE ANALYSIS; LIVER FAILURE; MITOCHONDRIAL ENERGY TRANSFER; MITOCHONDRIAL RESPIRATION; MUSCLE WEAKNESS; MYOPATHY; NONHUMAN; NUCLEOTIDE METABOLISM; OPHTHALMOPLEGIA; PATHOGENESIS; PHENOTYPE; PTOSIS; REGULATORY MECHANISM; REVIEW; SYNDROME; TISSUE SPECIFICITY; ANIMAL; ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETICS; GENOME; METABOLISM; MUTATION;

ANIMAL; DEOXYRIBONUCLEOSIDES; DNA, MITOCHONDRIAL; GENE DELETION; GENOME; HUMAN; MITOCHONDRIAL DISEASES; MUTATION; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); SYNDROME; THYMIDINE KINASE; ANIMALS; HUMANS;

EID: 0036019510     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-002-0343-5     Document Type: Review

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