The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.
Youssefian L, Vahidnezhad H, Barzegar M, Li Q, Sotoudeh S, Yazdanfar A, Ehsani AH, Kajbafzadeh AM, Mozafari N, Ebrahimi Daryani N, Agha-Hosseini F, Zeinali S, Uitto J.
Youssefian L, et al.
J Invest Dermatol. 2015 May;135(5):1447-1450. doi: 10.1038/jid.2015.9. Epub 2015 Jan 19.
J Invest Dermatol. 2015.
PMID: 25599393
Free article.
No abstract available.