Seven overlapping CNVs shared in >4 individuals with CoA were identified. The chromosome 21 CNV locus was present in all familial CoA cases. It contains TRPM2, which was also identified in the sporadi
Filtered variant call format (VCF) data of Jinbuol (JBO, female), Samgwang (SG, male), two RIL individuals (JSRIL1 and JSRIL2), Nipponbare1, IndicaHR12, Kitaake, and Kasalath using resequencing data p
The single nucleotide polymorphism (SNP) in the DRD2 gene ( DRD2 C939T ) was genotyped by PCR restriction fragment length polymorphism (PCR-RFLP). Finally, to ensure the reliability of the
