LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity

Published 2020 View Full Article

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Title
LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity
Authors
Keywords
-
Journal
MITOCHONDRION
Volume 51, Issue -, Pages 68-78
Publisher
Elsevier BV
Online
2020-01-07
DOI
10.1016/j.mito.2020.01.004

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