Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Epilepsy and PARK2[original query] |
---|
Rare structural genetic variation in human prion diseases. Neurobiology of aging 2015 May 36 (5): 2004.e1-8. Lukic Ana, Uphill James, Brown Craig A, Beck John, Poulter Mark, Campbell Tracy, Adamson Gary, Hummerich Holger, Whitfield Jerome, Ponto Claudia, Zerr Inga, Lloyd Sarah E, Collinge John, Mead Sim |
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients. Clinical neurology and neurosurgery 2021 Jan 202 106487. Albuz Burcu, Ozdemir Ozturk, Silan Fat |
- Page last reviewed:Feb 1, 2024
- Page last updated:Jun 11, 2024
- Content source: