A Prevalent Mutation with Founder Effect in Xeroderma Pigmentosum Group C from North Africa

Journal of Investigative Dermatology

Volumn 130, Issue 6, 2010, Pages 1537-1542

  Soufir, Nadem ^a   Ged, Cecile ^b,c,d   Bourillon, Agnes ^a   Austerlitz, Frederic ^e   Chemin, Cécile ^b,c,d   Stary, Anne ^f   Armier, Jacques ^f   Pham, Daniele ^f   Khadir, Khadija ^g   Roume, Joelle ^h   Hadj Rabia, Smail ⁱ   Bouadjar, Bakar ^j   Taieb, Alain ^b,c,d   De Verneuil, Hubert ^b,c,d   Benchiki, Hakima ^g   Grandchamp, Bernard ^a   Sarasin, Alain ^e  

^a BICHAT HOSPITAL   (France)

^b INSERM   (France)

^c UNIVERSITÉ DE BORDEAUX   (France)

^d HÔPITAL PELLEGRIN   (France)

^e UNIVERSITÉ PARIS SUD   (France)

^f Gustave Roussy Comprehensive Cancer Institute   (France)

^g IBN ROCHD UNIVERSITY HOSPITAL   (Morocco)

^h CENTRE HOSPITALIER INTERCOMMUNAL   (France)

ⁱ HÔPITAL NECKER ENFANTS MALADES   (France)

^j Bab El Oued Hospital   (Algeria)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; XERODERMA PIGMENTOSUM GROUP A PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; FEMALE; GENE SEQUENCE; GENETIC IDENTIFICATION; HAPLOTYPE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; NONSENSE MUTATION; NORTH AFRICA; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SOUTHERN EUROPE; XERODERMA PIGMENTOSUM;

EID: 77952419183     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2009.409     Document Type: Article

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