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A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma

Detalles Bibliográficos
Autores principales:	Kinsler, VA, Drury, S, Khan, A, Waelchli, R, Rukaite, G, Barnicoat, A, Lench, N, Harper, JI, O'Shaughnessy, RFL
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BlackWell Publishing Ltd 2015
Materias:	Research Letters
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303979/ https://www.ncbi.nlm.nih.gov/pubmed/25142840 http://dx.doi.org/10.1111/bjd.13361

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