All individuals with variants in gene KCND3

7 entries on 1 page. Showing entries 1 - 7.
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AscendingIndividual ID     

ID_report     

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VIP     

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Panel size     

Owner     
00103917 28327206-PatBH6435_1 PubMed: Eldomery 2017, Journal: Eldomery 2017 - - - United States - - - - - ? developmental delay, epilepsy, ataxia, mitochondrial dysfunction 1 1 Johan den Dunnen
00107885 - - - M - United States white - - - - SIDS sudden unexplained death syndrome 1 1 John Giudicessi
00107886 - - - M - United States African American - - - - SIDS sudden infant death syndrome 1 1 John Giudicessi
00107887 - - - M - United States white - - - - SIDS sudden unexplained death syndrome 1 1 John Giudicessi
00132965 - - - M - (Germany) - - - - - ? Delayed speech and language development (HP:0000750); Gait ataxia (HP:0002066) 1 1 IMGAG
00408677 Pat50 PubMed: Thomas 2022 no family history - no France - - - - - ? - 1 1 Johan den Dunnen
00453425 - - - F - - (not applicable) white - - - - ataxia HP:0007240, HP:0001250, HP:0001260, HP:0002015, HP:0000508, HP:0001268, HP:0002120, HP:0003473 1 1 Marketa Wayhelova
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