A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.

Br J Dermatol

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.

Published: January 2015

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303979PMC
http://dx.doi.org/10.1111/bjd.13361DOI Listing

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