All individuals with variants in gene SNTA1

10 entries on 1 page. Showing entries 1 - 10.
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VIP     

Data_av     

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Phenotype details     

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Owner     
00064738 - - - M - Denmark - 48y - - - SUD sudden unexplained death 1 1 Sofie Lindgren Christiansen
00128397 99 PubMed: Sahlin 2019, Journal: Sahlin 2019 stillbirth cohort (290 cases from Sweden) M - Sweden - - - - - ? - 1 1 Ellika Sahlin
00128443 197 PubMed: Sahlin 2019, Journal: Sahlin 2019 stillbirth cohort (290 cases from Sweden) M - Sweden - - - - - ? - 1 1 Ellika Sahlin
00128485 280 PubMed: Sahlin 2019, Journal: Sahlin 2019 stillbirth cohort (290 cases from Sweden) M - Sweden - - - - - ? - 1 1 Ellika Sahlin
00228665 son PubMed: van Kuilenburg 2018, Journal: van Kuilenburg 2018 - M - Netherlands - - - - - DPDD see paper; ..., born with apparent cortical blindness, subsequently exhibited severe developmental delay; 2y-severe spasticity, hyperreflexia felt secondary to intrauterine stroke; multiple brain MRIs delay in myelination; 18y-spastic paraparesis, mild intellectual disability 2 1 Johan den Dunnen
00292911 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 67 Mohammed Faruq
00292912 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00292913 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304851 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00453267 Fam136Pat156 Fusco 2042, submitted - M - Italy white - - - - CM - 1 1 Carmela Fusco
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