P. J. Dopping-Hepenstal

A functional "knockout" of human keratin 14.

E.L. Rugg, W.H. Irwin McLean, E. Birgitte Lane et al. · Genes & Development · 1994 · 177 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis

Bernhard Korge, Akemi Ishida‐Yamamoto, Claudia Pünter et al. · Journal of Investigative Dermatology · 1997 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Prenatal diagnosis for severe inherited skin disorders: 25 years' experience

Hiva Fassihi, Robin A.J. Eady, Jemima E. Mellerio et al. · British Journal of Dermatology · 2005 · 101 citations

Medicine, Dermatology, Genetics +17

A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

K. Batta, E.L. Rugg, N.J. Wilson et al. · British Journal of Dermatology · 2000 · 50 citations

Medicine, Dermatology, Genetics +13

Transient bullous dermolysis of the newborn in three generations

Hiva Fassihi, V. C. Diba, Vesarat Wessagowit et al. · British Journal of Dermatology · 2005 · 41 citations

Medicine, Dermatology, Pathology +17