Data related to article "Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions"
收藏NIAID Data Ecosystem2026-03-12 收录
下载链接：
https://zenodo.org/record/4604504
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资源简介：
Dataset includes VCF files containing the list of all the genomic variants found in P1 (whole exome) and in P2 (customized gene panel) by NGS analysis.
创建时间：
2021-04-15
