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Preliminary study on pathogenic mechanism of first Chinese family with PNKD
- Source :
- Translational Neuroscience, Vol 13, Iss 1, Pp 125-133 (2022)
- Publication Year :
- 2022
- Publisher :
- De Gruyter, 2022.
-
Abstract
- The first Chinese family with paroxysmal non-kinesigenic dystonia (PNKD) was confirmed to harbour a PNKD mutation. However, the pathogenic mechanism of the PNKD-causing gene mutation was unclear.
Details
- Language :
- English
- ISSN :
- 20816936
- Volume :
- 13
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Translational Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.5d2dd5a97f394a9381804d9ae790f36e
- Document Type :
- article
- Full Text :
- https://doi.org/10.1515/tnsci-2022-0222