The pathogenic A4269G mutation in human mitochondrial tRNAIlealters the T-stem structure and decreases the binding affinity for elongation factor Tu
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1356-9597.2004.00718.x/fullpdf
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3. Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene;Degoul;Hum. Mol. Genet.,1998
4. The yeast counterparts of human ‘MELAS’ mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu;Feuermann;EMBO Report,2003
5. Molecular investigations on tRNAs involved in human mitochondrial disorders;Florentz;Biosci. Report,2002
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