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4. Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds. Faiyaz-Ul-Haque M; Al-Sayed MD; Faqeih E; Jamil M; Saeed A; Amoudi MS; Kaya N; Abalkhail H; Al-Abdullatif A; Rashed M; Al-Owain M; Peltekova I; Zaidi SH Ann Saudi Med; 2014; 34(2):107-14. PubMed ID: 24894778 [TBL] [Abstract][Full Text] [Related]
5. Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria. Peng W; Ma XW; Yang X; Zhang WQ; Yan L; Wang YX; Liu X; Wang Y; Feng ZC BMC Med Genet; 2018 Sep; 19(1):167. PubMed ID: 30217188 [TBL] [Abstract][Full Text] [Related]
6. A novel compound heterozygous mutation of the L2HGDH gene in a Chinese boy with L-2-hydroxyglutaric aciduria: case report and literature review. Zhang Y; Wang C; Yang K; Wang S; Tian G; Chen Y Neurol Sci; 2018 Oct; 39(10):1697-1703. PubMed ID: 29980873 [TBL] [Abstract][Full Text] [Related]
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9. [L-2-hydroxyglutaric aciduria caused by a new mutation in the L2HGDH gene]. Saifullina EV; Zakharova EY; Kurkina MV; Magzhanov RV; Gaisina EV; Zakirova EN Zh Nevrol Psikhiatr Im S S Korsakova; 2017; 117(4):81-85. PubMed ID: 28617386 [TBL] [Abstract][Full Text] [Related]
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