CSMD1 gene mutations can lead to familial Parkinson disease

Mutation of the CSMD1 gene, which encodes a protein that participates in complement activation and inflammation in the CNS, leads to familial Parkinson disease (PD) in the absence of other gene mutations, new research published in Neurology: Genetics suggests. Whole-exome sequencing was performed in two unrelated Spanish families with PD,…

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