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Publications by N.J. Wilson
Novel Mutations in Desmoglein 1: Focal Palmoplantar Keratoderma in Milder Phenotypes
British Journal of Dermatology
Dermatology
Medicine
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Focal Palmoplantar Keratoderma With Joint Keratoses
Punctate Palmoplantar Keratoderma Type 1
Mutations in the Keratin 9 Gene in Pakistani Families With Epidermolytic Palmoplantar Keratoderma
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Dermatology
Pathogenic FAM83G Palmoplantar Keratoderma Mutations Inhibit the PAWS1:CK1α Association and Attenuate WNT Signalling.
Wellcome Open Research
Biochemistry
Medicine
Genetics
Molecular Biology
Hypopigmentation-Punctate Palmoplantar Keratoderma Syndrome
A Novel Missense Mutation in the Second Extracellular Domain of GJB2, p.Ser183Phe, Causes a Syndrome of Focal Palmoplantar Keratoderma With Deafness
American Journal of Pathology
Forensic Medicine
Pathology
Autosomal Recessive Palmoplantar Keratoderma and Congenital Alopecia
Hereditary Palmoplantar Keratoderma, Gamborg-Nielsen Type
Diffuse Palmoplantar Keratoderma With Painful Fissures
