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Year | Number of Results |
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2002 | 1 |
2016 | 2 |
2024 | 0 |
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Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
J Neurol Sci. 2016 May 15;364:116-21. doi: 10.1016/j.jns.2016.03.018. Epub 2016 Mar 12.
J Neurol Sci. 2016.
PMID: 27084228
SPAST mutation spectrum and familial occurrence among Czech patients with pure hereditary spastic paraplegia.
Mészárosová AU, Putzová M, Čermáková M, Vávrová D, Doležalová K, Smetanová I, Stejskal D, Beetz C, Seeman P.
Mészárosová AU, et al.
J Hum Genet. 2016 Oct;61(10):845-850. doi: 10.1038/jhg.2016.73. Epub 2016 Jun 23.
J Hum Genet. 2016.
PMID: 27334366
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Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
Sauter S, Miterski B, Klimpe S, Bönsch D, Schöls L, Visbeck A, Papke T, Hopf HC, Engel W, Deufel T, Epplen JT, Neesen J.
Sauter S, et al.
Hum Mutat. 2002 Aug;20(2):127-32. doi: 10.1002/humu.10105.
Hum Mutat. 2002.
PMID: 12124993
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