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A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.
Kinsler, V A; Drury, S; Khan, A; Waelchli, R; Rukaite, G; Barnicoat, A; Lench, N; Harper, J I; O'Shaughnessy, R F L.
Affiliation
  • Kinsler VA; Genetics and Genomic Medicine, UCL Institute of Child Health, 30 Guilford St, London, WC1N 1EJ, U.K; Paediatric Dermatology, Great Ormond St Hospital for Children, London, U.K.
Br J Dermatol ; 172(1): 262-4, 2015 Jan.
Article in En | MEDLINE | ID: mdl-25142840
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Genetic / Frameshift Mutation / Gene Deletion / Membrane Proteins Limits: Adult / Child / Female / Humans / Male Language: En Journal: Br J Dermatol Year: 2015 Document type: Article Affiliation country: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases, Genetic / Frameshift Mutation / Gene Deletion / Membrane Proteins Limits: Adult / Child / Female / Humans / Male Language: En Journal: Br J Dermatol Year: 2015 Document type: Article Affiliation country: United kingdom