All individuals with variants in gene SLC1A2

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

ID_report     

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VIP     

Data_av     

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Disease     

Phenotype details     

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Panel size     

Owner     
00089108 - - - M no Germany white >12y - - - epilepsy, focal, dysarthria, intellectual disability, cortical thickening, cerebellar atrophy - 1 1 Saskia Wortmann-Hagemann
00089198 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - F - - - - - - - EE early-onset epileptic encephalopathy 1 1 Johan den Dunnen
00089199 - PubMed: Epi4K consortium 2016, Journal: Epi4K consortium 2016 - F - - - - - - - EE early myoclonic encephalopathy 1 1 Johan den Dunnen
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