Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome

Publisher： Karger

E-ISSN： 1421-9832|228|2|183-188

ISSN： 1018-8665

Source： Dermatology, Vol.228, Iss.2, 2014-02, pp. : 183-188

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Clinico-Immunological Heterogeneity in Comèl-Netherton Syndrome

By  

Dermatology, Vol. 202, Iss. 2, 2001-04 ,pp. : 99-107

Karger

Access to resources Recommend Favorite

Bullous Pemphigoid in a Patient with Netherton’s Syndrome

By  

Dermatology, Vol. 214, Iss. 2, 2007-03 ,pp. : 183-185

Karger

Access to resources Recommend Favorite

Early Development of Multiple Epithelial Neoplasms in Netherton Syndrome

By  

Dermatology, Vol. 207, Iss. 2, 2003-08 ,pp. : 182-184

Karger

Access to resources Recommend Favorite

Netherton Syndrome with Extensive Skin Peeling and Failure to Thrive due to a Homozygous Frameshift Mutation in SPINK5

By  

Dermatology, Vol. 210, Iss. 4, 2005-05 ,pp. : 308-314

Karger

Access to resources Recommend Favorite

Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefèvre Syndrome

By  

Dermatology, Vol. 219, Iss. 4, 2009-10 ,pp. : 289-294

Karger

Access to resources Recommend Favorite