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Journal Article
Nature Genetics, ISSN 1061-4036, 11/2012, Volume 44, Issue 11, pp. 1272 - 1276
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 05/2011, Volume 131, Issue 5, pp. 1025 - 1028
Pachyonychia congenita (PC) is a rare, autosomal dominant keratin disorder caused by mutations in four genes ( , , , or ). The International PC Research... 
SUBSTITUTION | KERATIN-16 | TYPE-2 | STEATOCYSTOMA MULTIPLEX | DERMATOLOGY | Severity of Illness Index | Genetic Association Studies | Keratoderma, Palmoplantar - genetics | Humans | Pachyonychia Congenita - genetics | Child, Preschool | Keratin-16 - genetics | Male | Mutation - genetics | Pachyonychia Congenita - pathology | Quality of Life | Female | Child
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e64404
Journal Article
The Journal of investigative dermatology, ISSN 0022-202X, 3/2014, Volume 134, Issue 3, pp. 588 - 591
The International Pachyonychia Congenita Consortium (IPCC) was founded in 2004 in Park City, Utah, USA. Its goal is to find a cure for pachyonychia congenita,... 
keratin | pain | Pachyonychia congenita | nail | palmoplantar keratoderma
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 12, p. e28582
Journal Article