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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 8, 2024. (Total: 232338Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Seizures and POLG[original query]
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.
Epilepsia 2013 Jun 54 (6): 1002-11.
Uusimaa Johanna, Gowda Vasantha, McShane Anthony, Smith Conrad, Evans Julie, Shrier Annie, Narasimhan Manisha, O'Rourke Anthony, Rajabally Yusuf, Hedderly Tammy, Cowan Frances, Fratter Carl, Poulton Joan
Asymmetric Ataxia, Depression, Memory Loss, Epilepsy, and Axonal Neuropathy Associated with A Heterozygous DNA Polymerase Gamma Variant of Uncertain Significance, c1370G>a (R457Q).
Journal of neuromuscular diseases 2017 12 5 (1): 99-104.
Jerath Nivedita U, Shy Michael
POLG Mutations Are Probably Rare in the Han Chinese Population.
Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih 2021 1 35 (4): 350-356.
Yang Kun Fang, Meng Lin Yi, Zhang Yuan Feng, Yang Yong Chen, Cheng Hong Yi, Jiang Zhi Hu, Zhang Hong, Chen Yu C
Astrocytic pathology in Alpers' syndrome.
Acta neuropathologica communications 2023 5 11 (1): 86.
Laura A Smith, Chun Chen, Nichola Z Lax, Robert W Taylor, Daniel Erskine, Robert McFarla
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