Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Congenital Erythropoietic Porphyria[original query] |
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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria. Experimental dermatology 2005 1 14 (1): 50-5. de Villiers J Nico P, Kotze Maritha J, van Heerden Carel J, Sadie Annalene, Gardner Helena F J, Liebenberg Juanita, van Zyl René, du Plessis Lana, Kimberg Matti, Frank Jorge, Warnich Loui |
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