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 ...
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Dokumenttyp: | Artikel |
Erscheinungsdatum: | 2020 |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-29451379 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://repub.eur.nl/pub/125579 |