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CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder

CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder

Finsterer, Josef; Fiorini, Ana C.; Scorza, Carla A.; Scorza, Fulvio A.

期刊名称European Journal of Paediatric Neurology
作者Finsterer, Josef; Fiorini, Ana C.; Scorza, Carla A.; Scorza, Fulvio A.
印刷ISSN1090-3798
文件大小553.30KB
发表时间2018-4
DOI10.1016/j.ejpn.2018.04.012

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