Disrupted mitochondrial function in the Opa3...

Human Molecular Genetics 2016 / 04

Disrupted mitochondrial function in the Opa3 L122P mouse model for Costeff Syndrome impairs skeletal integrity

Navein, Alice E., Cooke, Esther J., Davies, Jennifer R., Smith, Terence G., Wells, Lois H. M., Ohazama, Atsushi, Healy, Christopher, Sharpe, Paul T., Evans, Sam L., Evans, Bronwen A. J., Votruba, Marc
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Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddw107
Date:
April, 2016
File:
PDF, 1.34 MB
english, 2016
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