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Number of items: 3.

Katugampola, Ruwani P., Badminton, Michael Norman, Finlay, Andrew Yule ORCID: https://orcid.org/0000-0003-2143-1646, Whatley, Sharon D., Woolf, Jacqueline ORCID: https://orcid.org/0000-0002-3009-9270, Mason, Nicola G., Deybach, J. C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X. and Anstey, Alexander Vincent ORCID: https://orcid.org/0000-0002-6345-4144 2012. Congenital erythropoietic porphyria: A single-observer clinical study of 29 cases. British Journal Of Dermatology 167 (4) , pp. 901-913. 10.1111/j.1365-2133.2012.11160.x

Katugampola, Ruwani P., Anstey, Alexander Vincent ORCID: https://orcid.org/0000-0002-6345-4144, Finlay, Andrew Yule ORCID: https://orcid.org/0000-0003-2143-1646, Whatley, Sharon D., Woolf, Jacqueline ORCID: https://orcid.org/0000-0002-3009-9270, Mason, Nicola G., Deybach, J. C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X. and Badminton, Michael Norman 2012. A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases. British Journal Of Dermatology 167 (4) , pp. 888-900. 10.1111/j.1365-2133.2012.11154.x

Whatley, Sharon D., Mason, Nicola G., Woolf, Jacqueline ORCID: https://orcid.org/0000-0002-3009-9270, Newcombe, Robert Gordon ORCID: https://orcid.org/0000-0003-4400-8867, Elder, George H. and Badminton, Michael Norman 2009. Diagnostic strategies for autosomal dominant acute porphyrias: retrospective analysis of 467 unrelated patients referred for mutational analysis of the HMBS, CPOX, or PPOX gene. Clinical Chemistry 55 (7) , pp. 1406-1414. 10.1373/clinchem.2008.122564

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