Molecular-Clinical Correlation in a Family With a Novel Heteroplasmic Leigh Syndrome Missense Mutation in the Mitochondrial Cytochrome c Oxidase III Gene
2010 ◽
Vol 26
(1)
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pp. 12-20
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Keyword(s):
2015 ◽
Vol 114
(5)
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pp. 1761-1768
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1992 ◽
Vol 267
(34)
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pp. 24273-24278
2012 ◽
Vol 26
(2)
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pp. 81-89
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2015 ◽
Vol 119
(2)
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pp. 157-157
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2018 ◽
Vol 10
(12)
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pp. 6811-6818
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