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One or more keywords matched the following properties of Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.

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has minor subject area list Bardet-Biedl Syndrome; Calcium Channels; Cell Line; Cerebellar Ataxia; DNA Methylation; Gene Expression; Humans; Polymorphism, Single Nucleotide; Proteins; Rare Diseases; Regulatory Sequences, Nucleic Acid; Sequence Analysis, RNA; Whole Genome Sequencing

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  • rare diseases