Metabolic and Organelle Morphology Defects in Mice and Human Patients Define Spinocerebellar Ataxia Type 7 as a Mitochondrial Disease

Published 2019 View Full Article

Authors

Keywords

spinocerebellar ataxia, polyglutamine, trinucleotide repeat, mitochondria, oxidative metabolism, nicotinamide adenine dinucleotide, Purkinje cell, ataxin-7, mouse model, induced pluripotent stem cells

Journal

Cell Reports

Volume 26, Issue 5, Pages 1189-1202.e6

Publisher

Elsevier BV

Online

2019-01-30

DOI

10.1016/j.celrep.2019.01.028

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