Nuclear genetic defects of mitochondrial ATP synthase

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F14%3A00428160" target="_blank" >RIV/67985823:_____/14:00428160 - 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

Nuclear genetic defects of mitochondrial ATP synthase

Original language description

The review summarizes current knowledge about nuclear genes mutations leading to the isolated deficiency of mitochondrial ATP synthase. Mutations in TMEM70, ATPAF1, ATP5A1 and ATP5E genes are discussed in the view of their prevalency in population and oftheir impact on the structure and function of ATP synthase

Czech name

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Czech description

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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

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2014

Confidentiality

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

Name of the periodical

Physiological Research

ISSN

0862-8408

e-ISSN

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Volume of the periodical

63

Issue of the periodical within the volume

Suppl.1

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

15

Pages from-to

"S57"-"S71"

UT code for WoS article

000332073100007

EID of the result in the Scopus database

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