A novel nicastrin mutation in a three-generation Dutch family with hidradenitis suppurativa: a search for functional significance

Background: Mutations in the γ-secretase enzyme subunits have been described in multiple kindreds with familial hidradenitis suppurativa (HS). Objective: In this study, we report a novel nicastrin (NCSTN) mutation causing HS in a Dutch family. We sought to explore the immunobiological function of NCSTN mutations using data of the Immunological Genome Project. Methods: Blood samples of three affected and two unaffected family members were collected. Whole-genome sequencing was performed using genomic DNA isolated from peripheral blood leucocytes. Sanger sequencing was done to confirm the causat... Mehr ...

Verfasser: Vossen, A.R.J.V. (Allard)
Straalen, K.R. (Kelsey) van
Swagemakers, S.M.A. (Sigrid)
de Klein, J.E.M.M. (J. E.M.M.)
Stubbs, A.P. (Andrew)
Venter, D. (Deon)
Zee, H.H. (Hessel) van der
Spek, P.J. (Peter) van der
Prens, E.P. (Errol)
Dokumenttyp: Artikel
Erscheinungsdatum: 2020
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29451379
Datenquelle: BASE; Originalkatalog
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Link(s) : http://repub.eur.nl/pub/125579