Failure to find evidence for deletion of LCE3C and LCE3B genes at PSORS4 contributing to psoriasis susceptibility in Tunisian families

Pathologie Biologie

Volumn 62, Issue 1, 2014, Pages 34-37

  Ammar, M ^a   Bouchlaka Souissi, C ^a   Soumaya, K ^a   Bouhaha, R ^a   Ines, Z ^b   Bouazizi, F ^a   Doss, N ^c   Dhaoui, R ^c   Ben Osman, A ^b   Ben Ammar El Gaaied A ^a   Mokni, M ^b   Marrakchi, R ^a  

^a FACULTÉ DES SCIENCES DE TUNIS   (Tunisia)

^b LA RABTA HOSPITAL   (Tunisia)

^c MILITARY HOSPITAL OF TUNIS   (Tunisia)

Author keywords

Copy number variation; Family based association study; Gene interaction; Genetics; Psoriasis

Indexed keywords

COPY NUMBER VARIATION; ÉTUDE D'ASSOCIATION BASÉE SUR DES FAMILLES; FAMILY-BASED ASSOCIATION STUDY; GENE INTERACTION; GENETICS; GÉNÉTIQUE; INTERACTION GÈNE-GÈNE; PSORIASIS; VARIATION DE NOMBRE DE COPIES;

ADOLESCENT; ADULT; AGED; CHILD; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; CORNIFIED ENVELOPE PROLINE-RICH PROTEINS; EPISTASIS, GENETIC; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HLA-C ANTIGENS; HUMANS; INDEL MUTATION; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PSORIASIS; SEQUENCE DELETION; TUNISIA; YOUNG ADULT;

EID: 84894245965     PISSN: 03698114     EISSN: 17683114     Source Type: Journal    
DOI: 10.1016/j.patbio.2013.10.003     Document Type: Article

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