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Query Trace: Epidermolysis Bullosa Simplex and KRT14[original query]

Known and novel mutations responsible for epidermolysis bullosa simplex cases in a Chinese population. Experimental and therapeutic medicine 2019 11 18 (6): 4661-4664. Zhang Jia, Ding Yu, Li Ming, Yao Zhirong, Zhuang Y Similar articles in PubMed
Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation. Journal of applied genetics 2015 Oct . Wertheim-Tysarowska K, O?dak M, Giza A, Kutkowska-Ka?mierczak A, Sota J, Przybylska D, Wo?niak K, ?niegórska D, Niepokój K, Sobczy?ska-Tomaszewska A, Rygiel A M, P?oski R, Bal J, Kowalewski Similar articles in PubMed
Mutations in KRT5 and KRT14 cause epidermolysis bullosa simplex in 75% of the patients. The British journal of dermatology 2011 Mar 164 (3): 637-44. Bolling M C, Lemmink H H, Jansen G H L, Jonkman M Similar articles in PubMed
Novel and recurrent mutations in Keratin 5 and 14 in Korean patients with Epidermolysis bullosa simplex. Journal of dermatological science 2010 1 57 (2): 90-4. Kang Tae-Won, Lee Jeong Seon, Kim Song-Ee, Oh Se-Woong, Kim Soo-Ch Similar articles in PubMed