(Q28288554)

2

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T A Dailey

3

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R R Morgan

4

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S D Whatley

5

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H A Dailey

6

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P Martasek

7

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Y Nordmann

8

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J C Deybach

9

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G H Elder

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

10

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language of work or name

English

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publication date

November 1998

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published in

Human Molecular Genetics

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volume

7

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issue

12

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page(s)

1921-5

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1 reference

The human protoporphyrinogen oxidase gene (PPOX): organization and location to chromosome 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Variegate porphyria: identification of a nonsense mutation in the protoporphyrinogen oxidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Homozygous variegate porphyria: an evolving clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Homozygous variegate porphyria: two similar cases in unrelated families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Homozygous variegate porphyria: identification of mutations on both alleles of the protoporphyrinogen oxidase gene in a severely affected proband

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Molecular analysis of the androgen-receptor gene in a family with receptor-positive partial androgen insensitivity: an unusual type of intronic mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Hepatic porphyrias in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Human protoporphyrinogen oxidase: expression, purification, and characterization of the cloned enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Homozygous variegate porphyria: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921

Site-directed mutagenesis of virtually any plasmid by eliminating a unique site

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.12.1921