Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases is a research paper published in medRxiv (2024). On theSindex it has a DataRank of 0.104. It has been cited 1 time.
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Base Score Contribution
0.104
From this paper's citation signal
Citation Network Contribution
0
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CORE--CLINICAL INTERFACE
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Precision Medicine for Inherited Retinal Degenerations
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