Steatocystoma multiplex is associated with the R94C mutation in the KRTl7 gene

Steatocystoma multiplex (SM) is an uncommon disorder, characterized by numerous skin-colored subcutaneous cysts. A number of SM pedigrees have been identified with mutations in the keratin 17 (KRT17) gene. The present study examined a four-generation Chinese pedigree with an autosomal dominant mode...

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Detalles Bibliográficos
Autores principales: LIU, QIAO, WU, WEIWEI, LU, JIEJIE, WANG, PING, QIAO, FENG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581757/
https://www.ncbi.nlm.nih.gov/pubmed/26165312
http://dx.doi.org/10.3892/mmr.2015.4063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581757/
https://www.ncbi.nlm.nih.gov/pubmed/26165312
http://dx.doi.org/10.3892/mmr.2015.4063

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