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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2012 | 2 |
2014 | 1 |
2024 | 0 |
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Page 1
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Nat Genet. 2011 Nov 20;43(12):1252-5. doi: 10.1038/ng.1008.
Nat Genet. 2011.
PMID: 22101681
Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.
Dale RC, Gardiner A, Antony J, Houlden H.
Dale RC, et al.
Dev Med Child Neurol. 2012 Oct;54(10):958-60. doi: 10.1111/j.1469-8749.2012.04394.x. Epub 2012 Jul 31.
Dev Med Child Neurol. 2012.
PMID: 22845787
Free article.
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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.
Heron SE, Grinton BE, Kivity S, Afawi Z, Zuberi SM, Hughes JN, Pridmore C, Hodgson BL, Iona X, Sadleir LG, Pelekanos J, Herlenius E, Goldberg-Stern H, Bassan H, Haan E, Korczyn AD, Gardner AE, Corbett MA, Gécz J, Thomas PQ, Mulley JC, Berkovic SF, Scheffer IE, Dibbens LM.
Heron SE, et al.
Am J Hum Genet. 2012 Jan 13;90(1):152-60. doi: 10.1016/j.ajhg.2011.12.003.
Am J Hum Genet. 2012.
PMID: 22243967
Free PMC article.
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PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia.
Wu L, Tang HD, Huang XJ, Zheng L, Liu XL, Wang T, Wang JY, Cao L, Chen SD.
Wu L, et al.
Parkinsonism Relat Disord. 2014 Dec;20(12):1399-404. doi: 10.1016/j.parkreldis.2014.10.012. Epub 2014 Oct 19.
Parkinsonism Relat Disord. 2014.
PMID: 25457817
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