Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening-Reference-Cited by-同舟云学术

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

Author:

Lovgren M.-L.¹,McAleer M.A.²³,Irvine A.D.²³⁴,Wilson N.J.⁵,Tavadia S.¹,Schwartz M.E.⁶,Cole C.⁷,Sandilands A.⁵,Smith F.J.D.⁵⁶,Zamiri M.¹⁸

Affiliation:

1. Department of Dermatology; University Hospital Crosshouse; Kilmarnock U.K

2. Department of Dermatology; Our Lady's; Children's Hospital Crumlin; Dublin Ireland

3. National Children's Research Centre; Children's Hospital Crumlin; Dublin Ireland

4. Clinical Medicine; Trinity College Dublin; Dublin Ireland

5. Dermatology and Genetic Medicine; Division of Biological Chemistry and Drug Discovery; University of Dundee; Dundee U.K

6. Pachyonychia Congenita Project; Salt Lake City UT U.S.A

7. Division of Computational Biology; School of Life Sciences; University of Dundee; Dundee U.K

8. Alan Lyell Centre for Dermatology; Queen Elizabeth University Hospital; Glasgow U.K

Funder

Pachyonychia Congenita Project

Wellcome Trust

Publisher

Wiley

Subject

Dermatology

Link

Reference17 articles.

1. Palmoplantar keratodermas;Itin;Clin Dermatol,2005

2. Molecular genetics of the inherited disorders of cornification: an update;Irvine;Adv Dermatol,2002

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