共济失调
医学
疾病
三核苷酸重复扩增
民族
脆性x
听力学
病理
精神科
遗传学
生物
政治学
等位基因
基因
法学
作者
Shen-Yang Lim,Hiroyuki Ishiura,Norlisah Ramli,Shota Shibata,M. Asem Almansour,Ai Lyn Tan,Henry Houlden,Anthony E. Lang,Shoji Tsuji
标识
DOI:10.1016/j.parkreldis.2020.03.025
摘要
Two ethnic Chinese men with clinico-radiologic features of Fragile X-associated tremor-ataxia syndrome (FXTAS) were found on genetic testing to have neuronal intranuclear inclusion disease (NIID), highlighting that NIID should be considered in the differential diagnosis of FXTAS. NIID may also be much more common than FXTAS in certain Asian populations.
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