Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease is a research paper published in Human Molecular Genetics (2022). On theSindex it has a DataRank of 0.524. It has been cited 32 times.
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Base Score Contribution
0.524
From this paper's citation signal
Citation Network Contribution
0
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This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
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Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals