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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1978 | 1 |
2011 | 1 |
2016 | 2 |
2024 | 0 |
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Page 1
Mutations in prickle orthologs cause seizures in flies, mice, and humans.
Am J Hum Genet. 2011 Feb 11;88(2):138-49. doi: 10.1016/j.ajhg.2010.12.012. Epub 2011 Feb 3.
Am J Hum Genet. 2011.
PMID: 21276947
Free PMC article.
Response to Sandford et al.: PRICKLE2 Variants in Epilepsy: A Call for Precision Medicine.
Mahajan VB, Bassuk AG.
Mahajan VB, et al.
Am J Hum Genet. 2016 Mar 3;98(3):590-591. doi: 10.1016/j.ajhg.2016.02.002.
Am J Hum Genet. 2016.
PMID: 26942292
Free PMC article.
No abstract available.
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Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.
Bird TD, Shaw CM.
Bird TD, et al.
J Neurol Neurosurg Psychiatry. 1978 Feb;41(2):140-9. doi: 10.1136/jnnp.41.2.140.
J Neurol Neurosurg Psychiatry. 1978.
PMID: 632821
Free PMC article.
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PRICKLE2 Mutations Might Not Be Involved in Epilepsy.
Sandford E, Bird TD, Li JZ, Burmeister M.
Sandford E, et al.
Am J Hum Genet. 2016 Mar 3;98(3):588-589. doi: 10.1016/j.ajhg.2016.01.009.
Am J Hum Genet. 2016.
PMID: 26942291
Free PMC article.
No abstract available.
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