Absence of pathogenic γ-secretase mutations in a South Wales cohort of familial and sporadic hidradenitis suppurativa (acne inversa)
Authors:
- 7 March 2013
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 168 (4) , 874-876
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Mutations in the γ-Secretase Genes NCSTN, PSENEN, and PSEN1 Underlie Rare Forms of Hidradenitis Suppurativa (Acne Inversa)Journal of Investigative Dermatology, 2012
- A novel splice site mutation inNCSTNunderlies a Japanese family with hidradenitis suppurativaBritish Journal of Dermatology, 2012
- Nicastrin Mutations in French Families with Hidradenitis SuppurativaJournal of Investigative Dermatology, 2012
- Two novel mutations of the nicastrin gene in Chinese patients with acne inversaBritish Journal of Dermatology, 2011
- PSENEN and NCSTN Mutations in Familial Hidradenitis Suppurativa (Acne Inversa)Journal of Investigative Dermatology, 2011
- Confirmation by Exome Sequencing of the Pathogenic Role of NCSTN Mutations in Acne Inversa (Hidradenitis Suppurativa)Journal of Investigative Dermatology, 2011
- γ-Secretase gene mutations link acne inversa with Alzheimer’s diseaseBritish Journal of Dermatology, 2011
- γ-Secretase Gene Mutations in Familial Acne InversaScience, 2010
- Presenilin 1 Glu318Gly PolymorphismArchives of Neurology, 2005
- The clinical genetics of hidradenitis suppurativa revisitedBritish Journal of Dermatology, 2000