Chromosome 18 (Human): Chromosome, Base pair, Gene, Cell (biology), Erythropoietic protoporphyria, Hereditary hemorrhagic telangiectasia, Niemann-Pick disease, Porphyria

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Chromosome 18 (Human): Chromosome, Base pair, Gene, Cell (biology), Erythropoietic protoporphyria, Hereditary hemorrhagic telangiectasia, Niemann-Pick disease, Porphyria

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Chromosome 18 (Human): Chromosome, Base pair, Gene, Cell (biology), Erythropoietic protoporphyria, Hereditary hemorrhagic telangiectasia, Niemann-Pick disease, Porphyria

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Brand OmniScriptum
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  • 9786132892591

OmniScriptum

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Gunther Disease: Congenital disorder, Erythropoietic porphyria, Inborn error of metabolism, Uroporphyrinogen III synthase, Chromosome

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VDM Verlag

NPC1L1: Niemann-Pick Disease, Protein, Gene

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