DNA helicases and human diseases;ADN hélicases et maladies associées

Medecine/Sciences

Volumn 22, Issue 12, 2006, Pages 1087-1094

  Uhring, Muriel ^a   Poterszman, Arnaud ^a  

^a INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE STRANDED DNA; RECQ HELICASE; SINGLE STRANDED DNA; WERNER SYNDROME PROTEIN; XERODERMA PIGMENTOSUM GROUP D PROTEIN;

BLOOM SYNDROME; CANCER SUSCEPTIBILITY; CATALYSIS; CLINICAL FEATURE; COCKAYNE SYNDROME; DNA STRAND BREAKAGE; ENZYME ACTIVITY; ENZYME DEFECT; FANCONI ANEMIA; GENE FUNCTION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; GENOMIC INSTABILITY; HUMAN; METABOLISM; REVIEW; ROTHMUND THOMSON SYNDROME; TRICHOTHIODYSTROPHY; WERNER SYNDROME; XERODERMA PIGMENTOSUM;

XERODERMA PIGMENTOSUM;

EID: 33845927856     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/200622121087     Document Type: Review

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