Literature DB >> 26211931

Mutations in EXPH5 underlie a rare subtype of autosomal recessive epidermolysis bullosa simplex.

E Rashidghamat1, L Ozoemena2, L Liu2, J A McGrath1, A E Martinez3, J E Mellerio1,3.   

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Year:  2015        PMID： 26211931     DOI： 10.1111/bjd.14047

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  2 in total

Review 1.  Raising Awareness Among Healthcare Providers about Epidermolysis Bullosa and Advancing Toward a Cure.

Authors:  Aaron Tabor; Joseph V Pergolizzi; Guy Marti; John Harmon; Bernard Cohen; Jo Ann Lequang
Journal:  J Clin Aesthet Dermatol       Date:  2017-05-01

Review 2.  Recently Identified Forms of Epidermolysis Bullosa.

Authors:  John A McGrath
Journal:  Ann Dermatol       Date:  2015-12-07       Impact factor: 1.444
  2 in total

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