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Fractal genetics and heterogeneous phenotypes of mitochondrial disease require appropriate logistics of managing network structures.

作者信息

Finsterer Josef

机构信息

Neurological Department, Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria.

出版信息

Mol Genet Metab Rep. 2019 Jul 5;20:100492. doi: 10.1016/j.ymgmr.2019.100492. eCollection 2019 Sep.

Abstract
摘要

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本文引用的文献

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Harmonizing care for rare diseases: How we developed the mitochondrial care network in the United States.
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MELAS syndrome due to the m.3291T > C mutation.
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Diagnosis of mitochondrial myopathies.
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Mitochondrial respiratory chain disorders I: mitochondrial DNA defects.
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