MFN2 mutations cause compensatory mitochondrial DNA proliferation
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F12%3A8188" target="_blank" >RIV/00064203:_____/12:8188 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11130/12:8188
Result on the web
<a href="http://dx.doi.org/10.1093/brain/aws049" target="_blank" >http://dx.doi.org/10.1093/brain/aws049</a>
DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
MFN2 mutations cause compensatory mitochondrial DNA proliferation
Original language description
MFN2 is the newest member of an expanding group of nuclear mitochondrial disorders characterized by disturbed mitochondrial DNA maintenance, a process which, increasingly, seems to be intrinsically related to the state of the mitochondrial network.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FH - Neurology, neuro-surgery, nuero-sciences
OECD FORD branch
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Result continuities
Project
<a href="/en/project/NS10554" target="_blank" >NS10554: Detection and analysis of mutations in mitofusin 2 gene (MFN2) as the known most common cause of axonal forms of hereditary neuropathies Charcot Marie Tooth (CMT 2).</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Brain
ISSN
0006-8950
e-ISSN
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Volume of the periodical
135
Issue of the periodical within the volume
Part 8
Country of publishing house
GB - UNITED KINGDOM
Number of pages
3
Pages from-to
1-3
UT code for WoS article
000307170300003
EID of the result in the Scopus database
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