Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disorder associated with heteroplasmic point mutations in the mitochondrial tRNA(Leu)(UUR) gene. While previous studies have shown that the MELAS mutation at nt-3243 results in impairments in...

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Xehetasun bibliografikoak
Argitaratua izan da:Nucleic Acids Res
Egile Nagusiak: Koga, Y, Davidson, M, Schon, E A, King, M P
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 1993
Sarrera elektronikoa:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC309166/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7680123/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/21.3.657
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