Acitretin therapy for Galli-Galli disease

Author:

Rundle Chandler W.,Ophaug Solveig,Simpson Eric L.

Funder

Pfizer

Publisher

Elsevier BV

Subject

Dermatology

Reference15 articles.

1. Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease;Basmanav;Am J Hum Genet,2014

2. Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease;Wilson;Br J Dermatol,2017

3. Genodermatose bei einem Brüderpaar: Morbus Dowling-Degos, Grover, Darier, Hailey-Hailey oder Galli-Galli? [Genodermatosis in a pair of brothers: Dowling-Degos, Grover, Darier, Hailey-Hailey or Galli-Galli disease?];Bardach;Hautarzt,1982

4. The spectrum of reticulate pigment disorders of the skin revisited;Müller;Eur J Dermatol,2012

5. Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease: Galli-Galli disease: a variant of Dowling-Degos disease?;Hanneken;Br J Dermatol,2010

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