A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy

Parkinsonism Relat Disord. 2018 Feb:47:91-93. doi: 10.1016/j.parkreldis.2017.12.005. Epub 2017 Dec 7.

¹ Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto, Catanzaro, Italy. Electronic address: g.nicoletti@unicz.it.
² Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto, Catanzaro, Italy.
³ Institute of Neurology, Department of Medical and Surgical Sciences, University Magna Graecia, Catanzaro, Italy.
⁴ Institute of Molecular Bioimaging and Physiology, National Research Council, Section of Germaneto, Catanzaro, Italy; Institute of Neurology, Department of Medical and Surgical Sciences, University Magna Graecia, Catanzaro, Italy.

No abstract available

Keywords: CHCHD2; MSA.

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