A Frameshift Mutation in PEN-2 Causes Familial Comedones Syndrome

Publisher： Karger

E-ISSN： 1421-9832|231|1|77-81

ISSN： 1018-8665

Source： Dermatology, Vol.231, Iss.1, 2015-05, pp. : 77-81

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

Expanding Phenotypic Spectrum of Familial Comedones

By  

Dermatology, Vol. 228, Iss. 3, 2014-05 ,pp. : 215-219

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

Familial Disseminated Comedones without Dyskeratosis: Report of an Affected Family and Review of the Literature

By  

Dermatology, Vol. 228, Iss. 4, 2014-05 ,pp. : 303-306

Karger

Access to resources Recommend Favorite

Unilateral Nodular Elastosis with Cysts and Comedones (Favre-Racouchot Syndrome)

By  

Dermatology, Vol. 202, Iss. 3, 2001-05 ,pp. : 270-271

Karger

Access to resources Recommend Favorite

Unilateral Nodular Elastosis with Cysts and Comedones (Favre-Racouchot Syndrome): Report of Two Cases Treated with a New Combined Therapeutic Approach

By  

Dermatology, Vol. 204, Iss. 3, 2002-05 ,pp. : 251-251

Karger

Access to resources Recommend Favorite