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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 2 |
2024 | 0 |
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Page 1
A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.
Arch Neurol. 2012 Sep;69(9):1190-2. doi: 10.1001/archneurol.2011.2600.
Arch Neurol. 2012.
PMID: 22964912
Free PMC article.
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.
Hirano M, Garone C, Quinzii CM.
Hirano M, et al.
Biochim Biophys Acta. 2012 May;1820(5):625-31. doi: 10.1016/j.bbagen.2012.01.006. Epub 2012 Jan 18.
Biochim Biophys Acta. 2012.
PMID: 22274133
Free PMC article.
Review.
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Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy.
Garone C, Tadesse S, Hirano M.
Garone C, et al.
Brain. 2011 Nov;134(Pt 11):3326-32. doi: 10.1093/brain/awr245. Epub 2011 Sep 20.
Brain. 2011.
PMID: 21933806
Free PMC article.
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