Rare pathogenic variants in IL36RN underlie a spectrum of psoriasis-associated pustular phenotypes

Journal of Investigative Dermatology

Volumn 133, Issue 5, 2013, Pages 1366-1369

  Setta Kaffetzi, Niovi ^a   Navarini, Alexander A ^a   Patel, Varsha M ^a   Pullabhatla, Venu ^a   Pink, Andrew E ^a   Choon, Siew Eng ^b   Allen, Michael A ^a   Burden, A David ^c   Griffiths, Christopher E M ^d   Seyger, Marieke M B ^e   Kirby, Brian ^f   Trembath, Richard C ^a,g   Simpson, Michael A ^a   Smith, Catherine H ^a   Capon, Francesca ^a   Barker, Jonathan N ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b HOSPITAL SULTANAH AMINAH   (Malaysia)

^c UNIVERSITY OF GLASGOW   (United Kingdom)

^d UNIVERSITY OF MANCHESTER   (United Kingdom)

^e RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^f ST VINCENT S UNIVERSITY HOSPITAL   (Ireland)

^g KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EXON; FRAMESHIFT MUTATION; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; IL36RN GENE; LETTER; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; PUSTULAR PSORIASIS; PUSTULOSIS PALMOPLANTARIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84876674307     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2012.490     Document Type: Letter

References (10)

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