Contribution of mtDNA heteroplasmy to 22q11.2 deletion syndrome phenotypes
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA636010
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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
