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Year | Number of Results |
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2007 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 614322
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The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.
Brain. 2014 Feb;137(Pt 2):411-9. doi: 10.1093/brain/awt338. Epub 2013 Dec 24.
Brain. 2014.
PMID: 24369382
Free PMC article.
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.
Gribaa M, Salih M, Anheim M, Lagier-Tourenne C, H'mida D, Drouot N, Mohamed A, Elmalik S, Kabiraj M, Al-Rayess M, Almubarak M, Bétard C, Goebel H, Koenig M.
Gribaa M, et al.
Brain. 2007 Jul;130(Pt 7):1921-8. doi: 10.1093/brain/awm078. Epub 2007 Apr 30.
Brain. 2007.
PMID: 17470496
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