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Letter|Research Support, Non-U.S. Gov't |
| endingPage |
403 |
| issn |
1353-8020 |
| issueIdentifier |
3 |
| pageRange |
402-403 |
| publicationName |
Parkinsonism & Related Disorders |
| startingPage |
402 |
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| bibliographicCitation |
Cai C, Shi O, Li WD. Missense mutations of the proline-rich transmembrane protein 2 gene cosegregate with mild paroxysmal kinesigenic dyskinesia and infantile convulsions in a Chinese pedigree. Parkinsonism Relat Disord. 2013 Mar;19(3):402–3. doi: 10.1016/j.parkreldis.2012.08.014. PMID: 23063574. |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0f6d90d4570dd4ea0a5d3b9960f1cbbd |
| date |
201303 |
| identifier |
https://doi.org/10.1016/j.parkreldis.2012.08.014
https://pubmed.ncbi.nlm.nih.gov/23063574 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21522 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Missense mutations of the proline-rich transmembrane protein 2 gene cosegregate with mild paroxysmal kinesigenic dyskinesia and infantile convulsions in a Chinese pedigree |
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