Homo sapiens mitochondrial twinkle protein gene, complete cds; nuclear - PopSet

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Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing. [Nucleic Acids Res. 2011]
Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.
Wang W, Shen P, Thiyagarajan S, Lin S, Palm C, Horvath R, Klopstock T, Cutler D, Pique L, Schrijver I, et al. Nucleic Acids Res. 2011 Jan; 39(1):44-58. Epub 2010 Sep 15.

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Homo sapiens isolate CHM13 chromosome 8, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 8, alternate assembly T2T-CHM13v2.0
gi|2194973728|gnl|ASM:GCF_009914825 f|NC_060932.1||gpp|GPC_000012747.1||gnl|NCBI_GENOMES|119568

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Homo sapiens mitochondrial twinkle protein gene, complete cds; nuclear gene for mitochondrial product.

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Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.

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