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Bonkovsky, Herbert
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Bonkovsky, Herbert
Item Type
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Concept
Genetic Diseases, X-Linked
Academic Article
Loss-of-function ferrochelatase and gain-of-function erythroid-specific 5-aminolevulinate synthase mutations causing erythropoietic protoporphyria and x-linked protoporphyria in North American patients reveal novel mutations and a high prevalence of X-linked protoporphyria.
Academic Article
Clinical, Biochemical, and Genetic Characterization of North American Patients With Erythropoietic Protoporphyria and X-linked Protoporphyria.
Search Criteria
Genetic Diseases X Linked