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Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria

Laurent Gouya   Caroline Martin-Schmitt   Anne-Marie Robreau  et al.
2006 January
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Erythropoietic protoporphyria (EPP) is an inherited disorder of heme biosynthesis that results from a partial deficiency of ferrochelatase (FECH).
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Periodical Source
Subject: Biology Title of Periodical:  American Journal of Human Genetics
Volume:  78 Issue:  1
Page(s):  2-14 Number of Volumes Cited:  1
CiteNumber:  251 Contributor:  jwalker
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APA Style

Gouya, L., Martin-Schmitt, C., & Robreau, A., etal. (2006). Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria. American Journal of Human Genetics, 78(1), 2-14.



MLA Style

Gouya, Laurent, Caroline Martin-Schmitt, and Anne-Marie Robreau, etal. ''Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria.'' American Journal of Human Genetics 78.1 (2006): 2-14.



Chicago Manual of Style

Gouya, Laurent, Caroline Martin-Schmitt and Anne-Marie Robreau, etal. ''Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria.'' American Journal of Human Genetics 78, no. 1 (2006): 2-14