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Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy.
Acta Neuropathol. 2020 Apr;139(4):791-794. doi: 10.1007/s00401-020-02128-8. Epub 2020 Jan 31.
Acta Neuropathol. 2020.
PMID: 32006098
No abstract available.
Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15).
Seidahmed MZ, Hamad MH, AlBakheet A, Elmalik SA, AlDrees A, Al-Sufayan J, Alorainy I, Ghozzi IM, Colak D, Salih MA, Kaya N.
Seidahmed MZ, et al.
BMC Neurol. 2020 May 25;20(1):207. doi: 10.1186/s12883-020-01761-w.
BMC Neurol. 2020.
PMID: 32450808
Free PMC article.
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