Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: A study of 17p11.2 rearrangements associated with CMT1A and HNPP

Human Molecular Genetics

Volumn 8, Issue 12, 1999, Pages 2285-2292

  Lopes, Judith ^a   Tardieu, Sandrine ^a   Silander, Kaisa ^b   Blair, Ian ^c   Vandenberghe, Antoon ^d   Palau, Francesco ^e   Ruberg, Merle ^a   Brice, Alexis ^a   LeGuern, Eric ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b UNIVERSITY OF TURKU   (Finland)

^c UNIVERSITY OF SYDNEY   (Australia)

^d Hopital de l'Antiquaille   (France)

^e HOSPITAL UNIVERSITARIO LA FE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE STRANDED DNA;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 17P; CHROMOSOME REARRANGEMENT; DNA REPAIR; DNA SEQUENCE; GENE CONVERSION; GENE DELETION; GENE DUPLICATION; GENETIC RECOMBINATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MAJOR CLINICAL STUDY; NEUROPATHY; NONHUMAN; PRIORITY JOURNAL; SISTER CHROMATID; YEAST;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOMES, HUMAN, PAIR 17; DNA; DNA DAMAGE; DNA REPAIR; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HETEROZYGOTE; HUMANS; MODELS, GENETIC; RECOMBINATION, GENETIC; SACCHAROMYCES CEREVISIAE;

EID: 0032695458     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.12.2285     Document Type: Article

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