CareLit · DOI-Nachweis · Aktuelle Neurologie
Genome-wide expression profiling of A3243G MELAS patients in quest for potential disease-modifying target genes
DOI 10.1055/s-2007-987636
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Autor:innenS Mende, A Herr, J Schmiedel, M Deschauer, T Klopstock, V Kostic, A Storch, H Reichmann
ZeitschriftAktuelle Neurologie
Ausgabe09/2007
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Mitochondrial encephalomyopathies represent an expanding group of clinical as well as genetical heterogeneous disorders caused by mitochondrial DNA (mtDNA) mutations or nuclear gene defects. The heteroplasmic mtDNA mutation at np 3243 (3243 A>G) in the tRNALeu(UUR) gene gives rise to one of the most frequent mitochondrial diseases, the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis and stroke-like…
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Zitierempfehlung
S Mende, A Herr, J Schmiedel, M Deschauer, T Klopstock, V Kostic, A Storch, H Reichmann (2007) Genome-wide expression profiling of A3243G MELAS patients in quest for potential disease-modifying target genes. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2007-987636
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