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Amanda Wilgoss
Amanda Wilgoss
Queen Mary University of London
Biology
Erythrokeratodermia variabilis
Mutation
Connexin
Palmoplantar keratoderma
3
Papers
183
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Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high‐performance liquid chromatography
2002
British Journal of Dermatology
Elizabeth L. Rugg
John E.A. Common
Amanda Wilgoss
H.P. Stevens
J Buchan
Irene M. Leigh
David P. Kelsell
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Citations (15)
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family.
2000
European Journal of Human Genetics
David P. Kelsell
Amanda Wilgoss
Gabriela Richard
Howard P. Stevens
Colin S. Munro
Irene M. Leigh
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Citations (99)
Identification of a Novel Mutation R42P in the Gap Junction Protein β-3 Associated with Autosomal Dominant Erythrokeratoderma Variabilis
1999
Journal of Investigative Dermatology
Amanda Wilgoss
Irene M. Leigh
Michael R. Barnes
Patricia J.C. Dopping-Hepenstal
Robin A.J. Eady
Joanne M Walter
C. T. C. Kennedy
David P. Kelsell
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Citations (69)
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