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Supplement: mmc4.xlsx › ALL
The human RNA polymerase I structure reveals an HMG-like docking domain specific to metazoans.
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Supplement: pcbi.1010013.s002.xlsx › _B__Y2H-SI_disMut_edgotypes
Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing.
Yan H et al.
Journal of Human Genetics, 2021
Combined Genome, Transcriptome and Metabolome Analysis in the Diagnosis of Childhood Cerebellar Ataxia.
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Mutation Edgotype Drives Fitness Effect in Human.
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Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants.
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Mechanisms of acquired resistance to rapalogs in metastatic renal cell carcinoma.
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Supplement: pgen.1007679.s001.xlsx › Table_S1
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