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Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease

✍ Scribed by Wang, Chaodong; Feng, Xiuli; Xie, Shu; Gu, Zhuqin; Chan, Piu


Book ID
122405683
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
139 KB
Volume
34
Category
Article
ISSN
0197-4580

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## Abstract Multiple genes have been now identified as causing Parkinson's disease (PD). In 2003, two mutations were identified in exon 1 of the Nurr1 gene in 10 of 107 individuals with familial PD. To date, investigators have only focused on screening for these known mutations of the Nurr1 gene. A