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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Epilepsy and SLC1A2[original query]
Influence of an interaction between lithium salts and a functional polymorphism in SLC1A2 on the history of illness in bipolar disorder.
Molecular diagnosis & therapy 2012 Oct 16 (5): 303-9.
Dallaspezia Sara, Poletti Sara, Lorenzi Cristina, Pirovano Adele, Colombo Cristina, Benedetti Frances
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy.
American journal of human genetics 2017 8 101 (2): 300-310.
Guella Ilaria, McKenzie Marna B, Evans Daniel M, Buerki Sarah E, Toyota Eric B, Van Allen Margot I, , Suri Mohnish, Elmslie Frances, , Simon Marleen E H, van Gassen Koen L I, Héron Delphine, Keren Boris, Nava Caroline, Connolly Mary B, Demos Michelle, Farrer Matthew
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.
Human genetics 2021 11 141 (1): 81-99.
Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous
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