Data related to article "Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions"
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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：
2021-03-15
