Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: SLC17A5[original query] |
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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. Brain : a journal of neurology 2017 Nov . Robak Laurie A, Jansen Iris E, van Rooij Jeroen, Uitterlinden André G, Kraaij Robert, Jankovic Joseph, , Heutink Peter, Shulman Joshua |
Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family. BMC medical genomics 2019 Nov 12 (1): 156. Lindholm Carlström Eva, Halvardson Jonatan, Etemadikhah Mitra, Wetterberg Lennart, Gustavson Karl-Henrik, Feuk La |
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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- Page last updated:Apr 22, 2024
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