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Therapeutics and Clinical Risk Management Volume 10, 2014 - Issue

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Letter

Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family

Zhiliang Li1 Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, People’s Republic of China

Qiao Liu2 Hainan Provincial Hospital of Skin Disease, Hainan, People’s Republic of China

Aimin Wang2 Hainan Provincial Hospital of Skin Disease, Hainan, People’s Republic of China

Hongsheng Wang1 Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, People’s Republic of China

Chengrang Li1 Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, People’s Republic of ChinaCorrespondence[email protected]

Pages 713-715 | Published online: 01 Sep 2014

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References

DiGiovannaJJBaleSJClinical heterogeneity in epidermolytic hyperkeratosisArch Dermatol19941308102610358053700
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YangJMNamKKimSWArginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosisJ Dermatol Sci199919212613310098704
PubMed Web of Science ®Google Scholar
SunXKMaLLXieYQZhuXJKeratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patientsJ Dermatol Sci200229319520012234709
PubMed Web of Science ®Google Scholar
ArinMJOjiVEmmertSExpanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosisBr J Dermatol2011164244244721271994
PubMed Web of Science ®Google Scholar

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