Literature DB >> 6838773

Dowling-Degos disease (reticulate pigmented anomaly of the flexures) is an autosomal dominant condition.

F Crovato, G Nazzari, A Rebora.   

Abstract

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Mesh：

Year:  1983        PMID： 6838773     DOI： 10.1111/j.1365-2133.1983.tb04602.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  3 in total

1.  Generalized dowling-degos disease: case reports.

Authors:  Jade Wititsuwannakul; Nopadon Noppakun
Journal:  Ann Dermatol       Date:  2013-08-13       Impact factor: 1.444

2.  Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.

Authors:  Regina C Betz; Laura Planko; Sibylle Eigelshoven; Sandra Hanneken; Sandra M Pasternack; Heinrich Bussow; Kris Van Den Bogaert; Joerg Wenzel; Markus Braun-Falco; Arno Rutten; Michael A Rogers; Thomas Ruzicka; Markus M Nöthen; Thomas M Magin; Roland Kruse
Journal:  Am J Hum Genet       Date:  2006-01-19       Impact factor: 11.025

Review 3.  The Genomic Architecture of Hidradenitis Suppurativa-A Systematic Review.

Authors:  Nikolai Paul Pace; Dillon Mintoff; Isabella Borg
Journal:  Front Genet       Date:  2022-03-23       Impact factor: 4.599
  3 in total

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