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Publications by David F. Bishop
Harderoporphyria Due to Homozygosity for Coproporphyrinogen Oxidase Missense Mutation H327R
Journal of Inherited Metabolic Disease
Genetics
Feline Congenital Erythropoietic Porphyria: Two Homozygous UROS Missense Mutations Cause the Enzyme Deficiency and Porphyrin Accumulation
Molecular Medicine
Molecular Medicine
Genetics
Molecular Biology
Design and Validation of an Open-Source Modular Microplate Photoirradiation System for High-Throughput Photobiology Experiments
PLoS ONE
Multidisciplinary
Uroporphyrinogen III Synthase Knock-In Mice Have the Human Congenital Erythropoietic Porphyria Phenotype, Including the Characteristic Light-Induced Cutaneous Lesions
American Journal of Human Genetics
Genetics
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