Litcius/Paper detail

Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review

Andrea Diociaiuti, Elisa Pisaneschi, Sabrina Rossi, Angelo Giuseppe Condorelli, Claudia Carnevale, Giovanna Zambruno, May El Hachem

2020Journal of the European Academy of Dermatology and Venereology13 citationsDOI

Topics & Concepts

MedicineEpidermolysis bullosaPediatricsDermatologySkin and Cellular Biology ResearchAutoimmune Bullous Skin DiseasesHair Growth and Disorders
Autosomal recessive epidermolysis bullosa simplex due to EXPH5 mutation: neonatal diagnosis of the first Italian case and literature review | Litcius