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Paper Details

Novel Indel Variation of NPC1 Gene Associates With Risk of Sudden Cardiac Death.
Front Genet
2
2022
1000G, 12-bp allele, 8-bp insertion/deletion polymorphism, C18orf8, NPC1, NPC1 Gene, Niemann-Pick, Niemann-Pick type C1 () gene, SCD, Sudden Cardiac Death, Sudden cardiac death, candidate, cardiac, cardiovascular diseases, deletion allele, deletion variant, eQTL, expression quantitative trait loci, human, human blood, human heart tissues, insertion allele, luciferase, mRNA, risk allele, rs150703258, unexpected death
Author NameAffiliation
Jianhua ZhangInstitute of Forensic Sciences
Jianhua ZhangInstitute of Forensic Sciences
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Release 1.2