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Details for: Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria.

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Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. [electronic resource]

By:

Wiman, Asa

Contributor(s):

Floderus, Ylva
Harper, Pauline

Producer: 20021009Description: 407-12 p. digitalISSN:

1434-5161

Subject(s):

Adult
Coproporphyrinogen Oxidase -- genetics
Female
Humans
Male
Middle Aged
Mutation, Missense
Pedigree
Polymorphism, Genetic
Porphyrias, Hepatic -- enzymology

Online resources:

Available from publisher's website

In: Journal of human genetics vol. 47

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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria.

APA

Wiman A., Floderus Y. & Harper P. (20021009). Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. : Journal of human genetics.

Chicago

Wiman Asa, Floderus Ylva and Harper Pauline. 20021009. Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. : Journal of human genetics.

Harvard

Wiman A., Floderus Y. and Harper P. (20021009). Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. : Journal of human genetics.

MLA

Wiman Asa, Floderus Ylva and Harper Pauline. Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. : Journal of human genetics. 20021009.

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