Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2

Journal of Investigative Dermatology

Volumn 128, Issue 6, 2008, Pages 1418-1422

  Liu, Ping ^a   Yang, Qingyu ^b   Wang, Xu ^a   Feng, Aiping ^a   Yang, Tao ^a   Yang, Rong ^a   Wang, Pengyun ^a   Yuang, Mingxiong ^a   Liu, Mugen ^a   Liu, Jing Yu ^a   Wang, Qing K ^a,c,d  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b First People's Hospital of Jiangxia District   (China)

^c LERNER RESEARCH INSTITUTE   (United States)

^d CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 10Q; CONTROLLED STUDY; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENOMICS; HUMAN; ICHTHYOSIS VULGARIS; PATHOGENESIS; PRIORITY JOURNAL;

EID: 43749100473     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5701191     Document Type: Article

References (13)

1. J.G. Compton J.J. DiGiovanna K.A. Johnston P. Fleckman S.J. Bale Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1 Exp Dermatol 11 2002 518 526
2. G.M. Lathrop J.M. Lalouel Easy calculations of lod scores and genetic risks on small computers Am J Hum Genet 36 1984 460 465
3. G. Lei Y. Zhang Y. Hu Investigation on the prevalence of ichthyosis in Sichuan province Chin J Dermatol 25 1992 105 106
4. T. Nomura A. Sandilands M. Akiyama H. Liao A.T. Evans K. Sakai Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis J Allergy Clin Immunol 119 2007 434 440
5. J.F. Okulicz R.A. Schwartz Hereditary and acquired ichthyosis vulgaris Int J Dermatol 42 2003 95 98
6. A. Sandilands A. Terron-Kwiatkowski P.R. Hull G.M. O'Regan T.H. Clayton R.M. Watson Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema Nat Genet 39 2007 650 654
7. T. Shwayder F. Ott All about ichthyosis Pediatr Clin North Am 38 1991 835 857
8. F.J. Smith A.D. Irvine A. Terron-Kwiatkowski A. Sandilands L.E. Campbell Y. Zhao Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris Nat Genet 38 2006 337 342
9. Q. Wang M.E. Curran I. Splawski T.C. Burn J.M. Millholland T.J. VanRaay Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias Nat Genet 12 1996 17 23
10. Q. Wang J. Shen I. Splawski D. Atkinson Z. Li J.L. Robinson SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome Cell 80 1995 805 811
11. R.S. Wells C.B. Kerr Clinical feature of autosomal dominant and sex-linked ichthyosis in an English population BMJ 1 1966 947 950
12. W. Zhong B. Cui Y. Zhang H. Jiang S. Wei L. Bu Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22 J Hum Genet 48 2003 390 392
13. L. Ziprkowski A. Feinstein A survey of ichthyosis vulgaris in Israel Br J Dermatol 86 1972 1 8