Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy is a research paper published in Annals of Clinical and Translational Neurology (2024). On theSindex it has a DataRank of 0. It has been cited 3 times.
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Common Fund
Grant: U01HG010218
National Human Genome Research Institute
Grant: UM1HG008900
National Human Genome Research Institute
Grant: R01 HG009141
NINDS NIH HHS
Grant: U01 NS134356
NINDS NIH HHS
Grant: K22 NS104135
National Institutes of Health
Grant: 3U01HG010218-04S2
Center for Undiagnosed Diseases at Stanford Administrative Supplement
National Institutes of Health
Grant: 5UM1HG008900-04
Joint Center for Mendelian Genomics
National Institutes of Health
Grant: 5R01HG009141-02
A powerful web-based discovery platform for rare disease genetics
Canadian Institutes of Health Research
Grant: unidentified
unidentified
Silicon Valley Community Foundation
National Institute of Neurological Disorders and Stroke
FWCI
0.88
Citation Percentile
0.7%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals