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Q41502419-FA71ACBF-D83A-4D02-A84B-7EE87155D08F
Q41502419-FA71ACBF-D83A-4D02-A84B-7EE87155D08F
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Statement
http://www.wikidata.org/entity/statement/Q41502419-FA71ACBF-D83A-4D02-A84B-7EE87155D08F
A disease-causing point mutation in human mitochondrial tRNAMet results in tRNA misfolding leading to defects in translational initiation and elongation.
P2860
Q41502419-FA71ACBF-D83A-4D02-A84B-7EE87155D08F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41502419-FA71ACBF-D83A-4D02-A84B-7EE87155D08F
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type
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wasDerivedFrom
9a99ce08199a8d603b7483adbca3c0e386b98e81
P2860
Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.