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3.044 VARIANT IN THE 3' REGION OF SNCA ASSOCIATED WITH PARKINSON'S DISEASE AND SERUM α-SYNUCLEIN LEVELS

✍ Scribed by Y. Hu; B. Tang; J. Guo; X. Wu; Q. Sun; L. Shen; X. Yan; C. Wang; L. Tan; H. Zhang


Book ID
117755147
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
73 KB
Volume
18
Category
Article
ISSN
1353-8020

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## Abstract Missense mutations of the α‐synuclein gene have been reported to explain a few kindreds with autosomal dominant Parkinson's disease (PD). In order to identify mutations in our PD patients, we have screened the coding region and 5′flanking region of the gene. DNA samples from 50 patients