Contribution of mtDNA heteroplasmy to 22q11.2 deletion syndrome phenotypes
收藏NIAID Data Ecosystem2026-03-11 收录
官方服务：
资源简介：
We sequenced the mtDNA of mother-child pairs affected by chromosome 22q11 microdeletion syndrome, and compared the intrafamilial allele frequency change between phenotypically concordant and discordant pairs.
创建时间：
2020-05-30
