Genetic analysis of NCSTN for potential association with hidradenitis suppurativa in familial and nonfamilial patients

Br J Dermatol. 2016 Aug;175(2):414-6. doi: 10.1111/bjd.14482. Epub 2016 Jun 10.

Authors

M Liu¹, J W Davis¹, K B Idler¹, N M Mostafa², M M Okun³, J F Waring¹

Affiliations

¹ Pharmacogenetics and Pharmacogenomics, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
² Research and Development, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
³ Department of Immunology, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.

PMID: 26879264
DOI: 10.1111/bjd.14482

No abstract available

Publication types

Letter

MeSH terms

Adolescent
Adult
Aged
Amyloid Precursor Protein Secretases / genetics*
Case-Control Studies
Clinical Trials, Phase III as Topic
Codon, Nonsense / genetics*
Female
Genetic Predisposition to Disease / genetics
Hidradenitis Suppurativa / genetics*
Humans
Male
Membrane Glycoproteins / genetics*
Middle Aged
Mutation, Missense / genetics*
Polymorphism, Single Nucleotide / genetics*
Sequence Analysis, DNA
White People / genetics
Young Adult

Substances

Codon, Nonsense
Membrane Glycoproteins
nicastrin protein
Amyloid Precursor Protein Secretases