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Genetic analysis of NCSTN for potential association with hidradenitis suppurativa in familial and nonfamilial patients.
Liu, M; Davis, J W; Idler, K B; Mostafa, N M; Okun, M M; Waring, J F.
Affiliation
  • Liu M; Pharmacogenetics and Pharmacogenomics, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
  • Davis JW; Pharmacogenetics and Pharmacogenomics, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
  • Idler KB; Pharmacogenetics and Pharmacogenomics, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
  • Mostafa NM; Research and Development, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
  • Okun MM; Department of Immunology, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
  • Waring JF; Pharmacogenetics and Pharmacogenomics, AbbVie Inc., One N. Waukegan Road, North Chicago, IL, 60064, U.S.A.
Br J Dermatol ; 175(2): 414-6, 2016 Aug.
Article in En | MEDLINE | ID: mdl-26879264

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Hidradenitis Suppurativa / Codon, Nonsense / Mutation, Missense / Polymorphism, Single Nucleotide / Amyloid Precursor Protein Secretases Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Dermatol Year: 2016 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Hidradenitis Suppurativa / Codon, Nonsense / Mutation, Missense / Polymorphism, Single Nucleotide / Amyloid Precursor Protein Secretases Type of study: Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Dermatol Year: 2016 Type: Article Affiliation country: United States