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Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease

✍ Scribed by Jin-yong Tian; Ji-feng Guo; Lei Wang; Qi-ying Sun; Ling-yan Yao; Lin-zi Luo; Chang-he Shi; Ya-cen Hu; Xin-xiang Yan; Bei-sha Tang

Book ID
116774078
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
537 KB
Volume
516
Category
Article
ISSN
0304-3940

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Frequency and phenotypes of LRRK2 G2019S
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✍ Roberta Marongiu; Daniele Ghezzi; Tamara Ialongo; Francesco Soleti; Antonio Elia πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 74 KB

To evaluate the frequency of the LRRK2 G2019S mutation in Italy, we tested 1,072 probands with Parkinson's disease (PD; 822 sporadic and 250 familial): 20 patients (1.9%) carried the G2019S mutation, 11 patients (1.3%) were sporadic, and 9 (4.3%) had a positive family history. Considering only proba