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Rintoul, Gordon

Altered mitochondrial dynamics in a novel cellular model of Leber Hereditary Optic Neuropathy (LHON)
Disruption of Kif5c mediated movement affects mitochondrial form, function and cellular health in rat primary cortical neurons and astrocytes
Mitochondrial form and function in patient-derived fibroblasts harbouring the G11778A mutation of Leber's hereditary optic neuropathy
Mitochondrial form and function: an investigation of the mechanism and significance of mitochondrial remodelling in rat cortical astrocytes

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Simon Fraser University Library is grateful to be located on the lands of the xʷməθkʷəy̓əm (Musqueam), Sḵwx̱wú7mesh (Squamish), səl̓ilw̓ətaʔɬ (Tsleil-Waututh), q̓íc̓əy̓ (Katzie), kʷikʷəƛ̓əm (Kwikwetlem), qiqéyt (Qayqayt), qʼʷa:n̓ƛʼən̓ (Kwantlen), Səmyámə (Semiahmoo), and sc̓əwaθən (Tsawwassen) Nations.

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