Associated Papers
Novel variants in LAMA3 and COL7A1 and recurrent variant in KRT5 underlying epidermolysis bullosa in five Chinese families.
Wang R et al.
Frontiers of Medicine, 2022
Enamel defects in carriers of a novel LAMA3 mutation underlying epidermolysis bullosa.
Yuen WY et al.
Acta Dermato-venereologica, 2012
Select a paper to view details