Mutations of the mitochondrial carrier translocase channel...

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Human Molecular Genetics 2018 / 09

Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy

Pacheu-Grau, David, Callegari, Sylvie, Emperador, Sonia, Thompson, Kyle, Aich, Abhishek, Topol, Sarah E, Spencer, Emily G, McFarland, Robert, Ruiz-Pesini, Eduardo, Torkamani, Ali, Taylor, Robert W, Mo
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Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddy305
Date:
September, 2018
File:
PDF, 6.37 MB
english, 2018
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