The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Nature Genetics

Volumn 37, Issue 9, 2005, Pages 934-935

  Levitus, Marieke ^a   Waisfisz, Quinten ^a   Godthelp, Barbara C ^b   De Vries, Yne ^a   Hussain, Shobbir ^c   Wiegant, Wouter W ^b   Elghalbzouri Maghrani, Elhaam ^b   Steltenpool, Jûrgen ^a   Rooimans, Martin A ^a   Pals, Gerard ^a   Arwert, Fré ^a   Mathew, Christopher G ^c   Zdzienicka, Małgorzata Z ^b,d   Hiom, Kevin ^e   De Winter, Johan P ^a   Joenje, Hans ^a  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c KING'S COLLEGE LONDON   (United Kingdom)

^d NICOLAUS COPERNICUS UNIVERSITY   (Poland)

^e MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; BRIP1 PROTEIN, HUMAN; DNA BINDING PROTEIN; MICROSATELLITE DNA; RNA HELICASE;

ARTICLE; CANCER RISK; CHROMOSOME; FANCONI ANEMIA; HUMAN; NONHUMAN; PATHOGENICITY; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; CHROMOSOME 17; GENE DELETION; GENETIC COMPLEMENTATION; GENETICS; MOLECULAR GENETICS; MUTATION;

CHROMOSOMES, HUMAN, PAIR 17; DNA-BINDING PROTEINS; FANCONI ANEMIA; GENETIC COMPLEMENTATION TEST; HUMANS; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUTATION; RNA HELICASES; SEQUENCE DELETION;

EID: 25144457604     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1625     Document Type: Article

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