Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon–Lefevre syndrome in a Saudi family

Papillon–Lefevre syndrome (PALS) is a rare, autosomal recessive disorder characterized by periodontitis and hyperkeratosis over the palms and soles. Mutations in the cathepsin C gene (CTSC) have been recognized as the cause of PALS since the late 1990s. More than 75 mutations in CTSC have been ident...

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Detalles Bibliográficos
Autores principales: Alkhiary, Yaser Mohammad, Jelani, Musharraf, Almramhi, Mona Mohammad, Mohamoud, Hussein Sheikh Ali, Al-Rehaili, Rayan, Al-Zahrani, Hams Saeed, Serafi, Rehab, Yang, Huanming, Al-Aama, Jumana Yousuf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992098/
https://www.ncbi.nlm.nih.gov/pubmed/27579005
http://dx.doi.org/10.1016/j.sjbs.2015.06.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992098/
https://www.ncbi.nlm.nih.gov/pubmed/27579005
http://dx.doi.org/10.1016/j.sjbs.2015.06.007

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