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Year | Number of Results |
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2007 | 1 |
2012 | 2 |
2013 | 2 |
2016 | 1 |
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Page 1
Myofibrillar myopathies: new developments.
Curr Opin Neurol. 2013 Oct;26(5):527-35. doi: 10.1097/WCO.0b013e328364d6b1.
Curr Opin Neurol. 2013.
PMID: 23995273
Free PMC article.
Review.
Filamin C-related myopathies: pathology and mechanisms.
Fürst DO, Goldfarb LG, Kley RA, Vorgerd M, Olivé M, van der Ven PF.
Fürst DO, et al.
Acta Neuropathol. 2013 Jan;125(1):33-46. doi: 10.1007/s00401-012-1054-9. Epub 2012 Oct 30.
Acta Neuropathol. 2013.
PMID: 23109048
Free PMC article.
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Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population.
Odgerel Z, Lee HS, Erdenebileg N, Gandbold S, Luvsanjamba M, Sambuughin N, Sonomtseren S, Sharavdorj P, Jodov E, Altaisaikhan K, Goldfarb LG.
Odgerel Z, et al.
J Diabetes. 2012 Sep;4(3):238-42. doi: 10.1111/j.1753-0407.2011.00177.x.
J Diabetes. 2012.
PMID: 22151254
Free PMC article.
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Genetic fitness and selection intensity in a population affected with high-incidence spinocerebellar ataxia type 1.
Platonov FA, Tyryshkin K, Tikhonov DG, Neustroyeva TS, Sivtseva TM, Yakovleva NV, Nikolaev VP, Sidorova OG, Kononova SK, Goldfarb LG, Renwick NM.
Platonov FA, et al.
Neurogenetics. 2016 Jul;17(3):179-85. doi: 10.1007/s10048-016-0481-5. Epub 2016 Apr 22.
Neurogenetics. 2016.
PMID: 27106293
Free PMC article.
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Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.
Olivé M, Armstrong J, Miralles F, Pou A, Fardeau M, Gonzalez L, Martínez F, Fischer D, Martínez Matos JA, Shatunov A, Goldfarb L, Ferrer I.
Olivé M, et al.
Neuromuscul Disord. 2007 Jun;17(6):443-50. doi: 10.1016/j.nmd.2007.02.009. Epub 2007 Apr 5.
Neuromuscul Disord. 2007.
PMID: 17418574
Free PMC article.
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