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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2018 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
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Fibulin-5 mutations link inherited neuropathies, age-related macular degeneration and hyperelastic skin.
Brain. 2011 Jun;134(Pt 6):1839-52. doi: 10.1093/brain/awr076. Epub 2011 May 15.
Brain. 2011.
PMID: 21576112
Free PMC article.
Genetic analysis of Charcot-Marie-Tooth disease in Denmark and the implementation of a next generation sequencing platform.
Vaeth S, Christensen R, Dunø M, Lildballe DL, Thorsen K, Vissing J, Svenstrup K, Hertz JM, Andersen H, Jensen UB.
Vaeth S, et al.
Eur J Med Genet. 2019 Jan;62(1):1-8. doi: 10.1016/j.ejmg.2018.04.003. Epub 2018 Apr 11.
Eur J Med Genet. 2019.
PMID: 29653220
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Fibulin-5 mutation featuring Charcot-Marie-Tooth disease, joint hyperlaxity, and scoliosis.
Kazamel M, Lopez MA, Bebin M, Bowling K, Korf BR, Barsh GS, Cooper GM, Hurst ACE, Ubogu EE.
Kazamel M, et al.
Neurol Genet. 2020 Jun 25;6(4):e476. doi: 10.1212/NXG.0000000000000476. eCollection 2020 Aug.
Neurol Genet. 2020.
PMID: 32802946
Free PMC article.
No abstract available.
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