Functional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter Deficiency is a research paper published in Proceedings of the National Academy of Sciences (2022). On theSindex it has a DataRank of 0.538. It has been cited 35 times.
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Base Score Contribution
0.538
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.
Learn more about DataRank methodology →Additional file 3 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 4 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 2 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 3 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 2 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 4 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 1 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Additional file 1 of Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis