Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy phenotype is a research paper published in Neuromuscular Disorders (2025). On theSindex it has a DataRank of 0.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph β no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full β never from an abstract alone.
NIAMS NIH HHS
Grant: P50 AR070604
NICHD NIH HHS
Grant: P50 HD117373
FWCI
0.00
Citation Percentile
0.2%
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Sustainable Development Goals