Article

The variant of CHCHD2 p.P2L in a familial case of Parkinson’s disease with poor response to levodopa therapy: A case report

2024-04-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold> Mutations in the coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) gene have been reported successively in sporadic and familial PD patients, presenting typical manifestations of primary Parkinson's disease (PD) and sensitive to levodopa therapy. This provides more clues to the genetic component of PD. <bold>Case presentations</bold> We reported a...

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Literature Corpus work: de693c5f-d26f-5f54-9247-3ac2e8da6087
DOI: 10.21203/rs.3.rs-4182809/v1

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