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Mutations inSMARCAD1cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes

  • Published:2014-10-26 Issue:6 Volume:171 Page:1521-1524
  • ISSN:0007-0963
  • Container-title:British Journal of Dermatology
  • language:en
  • Short-container-title:Br J Dermatol

Author:

Nousbeck J.1,Sarig O.1,Magal L.1,Warshauer E.1,Burger B.2,Itin P.23,Sprecher E.14

Affiliation:

1. Department of Dermatology; Tel Aviv Sourasky Medical Center; 6, Weizmann street Tel Aviv 64239 Israel

2. Department of Biomedicine; University Hospital Basel; Basel Switzerland

3. Department of Dermatology; University Hospital Basel; Basel Switzerland

4. Department of Human Molecular Genetics & Biochemistry; Tel-Aviv University; Tel Aviv Israel

Publisher

Wiley

Subject

Dermatology

Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Disorders of Collagen, Elastin and Dermal Matrix;Rook's Textbook of Dermatology;2024-02-20

2. Basan syndrome in a family from South India: a novel SMARCAD1 variant;Clinical and Experimental Dermatology;2023-11-15

3. Adermatoglyphia in the Era of Biometrics;Indian Journal of Dermatology;2022-07

4. Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma;Disease Markers;2022-05-10

5. La génétique des kératodermies palmoplantaires isolées;Annales de Dermatologie et de Vénéréologie - FMC;2022-03
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