Associated Papers
Novel Ala94Thr mutation of keratin 14 in epidermolysis bullosa simplex.
Zeng K et al.
International Journal of Dermatology, 2014
Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14.
Yiasemides E et al.
Clinical and Experimental Dermatology, 2008
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.
Lugassy J et al.
American Journal of Human Genetics, 2006
Novel keratin 14 mutations in patients with severe recessive epidermolysis bullosa simplex.
Has C et al.
The Journal of Investigative Dermatology, 2006
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