Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F05%3A00011031" target="_blank" >RIV/00216208:11110/05:00011031 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria

Original language description

hydrophobic cluster analysis, ocidase negne, heme biosynthesis, protein, sequence, information, metabolism

Czech name

Mutace v lidském CPO genu predikují klinický obraz jaterní hereditární koproporfyrie nebo erytropoetické harderoporfyrie

Czech description

protein, CPO gen

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

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Continuities

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Publication year

2005

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Human Molecular Genetics

ISSN

0964-6906

e-ISSN

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Volume of the periodical

14

Issue of the periodical within the volume

20

Country of publishing house

GB - UNITED KINGDOM

Number of pages

10

Pages from-to

3089-3098

UT code for WoS article

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EID of the result in the Scopus database

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