Author:
Rakowska Adriana,Rudnicka Lidia
Reference15 articles.
1. Neila Iglesias J, Rodriguez Pichardo A, Garcia Bravo B, Camacho Martinez F. Masquerading of trichotillomania in a family with monilethrix. Eur J Dermatol. 2011;21(1):133.
2. Djabali K, Panteleyev AA, Lalin T, Garzon MC, Longley BJ, Bickers DR, et al. Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix. Clin Exp Dermatol. 2003;28(2):206–10.
3. Shimomura Y, Sakamoto F, Kariya N, Matsunaga K, Ito M. Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis. J Invest Dermatol. 2006;126(6):1281–5.
4. Farooq M, Ito M, Naito M, Shimomura Y. A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene. Br J Dermatol. 2011;165(2):425–31.
5. Zlotogorski A, Marek D, Horev L, Abu A, Ben-Amitai D, Gerad L, et al. An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis. J Invest Dermatol. 2006;126(6):1292–6.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献