LRRK2
基因型
疾病
帕金森病
医学
突变
内科学
人口
队列
发病年龄
胃肠病学
遗传学
生物
基因
环境卫生
作者
Ziv Gan‐Or,Nir Giladi,U. Rozovski,C. Shifrin,Serena Rosner,Tanya Gurevich,Anat Bar‐Shira,Avi Orr‐Urtreger
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2008-04-24
卷期号:70 (24): 2277-2283
被引量:355
标识
DOI:10.1212/01.wnl.0000304039.11891.29
摘要
These data demonstrate genotype-phenotype correlations between different GBA mutations and Parkinson disease (PD) risk and AAO in Ashkenazi Jews. Additionally, an earlier AAO was observed in LRRK2 G2019S carrier PD patients. Finally, these data demonstrate that a surprisingly high frequency, more than one third of our patient population, carried a mutation in GBA or LRRK2.
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