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

Mitochondrion - Tập 51 - Trang 68-78 - 2020
Arnaud Besse1, Daniel Brezavar1, Jennifer Hanson1, Austin Larson2, Penelope E. Bonnen1
1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
2University of Colorado School of Medicine and Children’s Hospital Colorado, Aurora, CO, United States

Tài liệu tham khảo

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