Loss-of-function mutation inAAGABin Chinese families with punctuate palmoplantar keratoderma

Author:

Li M.1,Yang L.2,Shi H.3,Guo B.4,Dai X.2,Yao Z.1,Zhang G.3

Affiliation:

1. Department of Dermatology; Xinhua Hospital; Shanghai Jiaotong University School of Medicine; 1665 Kongjiang Road Shanghai 200092 China

2. Department of Dermatology; Wuxi No. 2 People's Hospital; Jiangsu China

3. Department of Dermatology; Wuxi People's Hospital; Wuxi, Jiangsu China

4. Department of Dermatology; the Third Affiliated Hospital of Anhui Medical University and the First People's Hospital of Hefei; Anhui China

Publisher

Wiley

Subject

Dermatology

Reference12 articles.

1. 47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer;Emmert;Eur J Dermatol,2003

2. Identification of a locus for punctate palmoplantar keratodermas at chromosome 8q24.13-8q24.21;Zhang;J Invest Dermatol,2004

3. Hereditary palmoplantar keratoderma, type papulosa, in Croatia;Stanimirovic;J Am Acad Dermatol,1993

4. Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24;Martinez-Mir;J Med Genet,2003

5. Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31;Gao;Br J Dermatol,2005

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