LRRK2
遗传学
疾病
外显子
医学
突变
帕金森病
基因
遗传咨询
生物
内科学
作者
Jaya Sanyal,Biswanath Sarkar,Sabyasachi Ojha,Tapas Kumar Banerjee,Jayanta K. Ray,Vadlam Raghavendra Rao
出处
期刊:Genetic Testing and Molecular Biomarkers
[Mary Ann Liebert, Inc.]
日期:2010-08-19
卷期号:14 (5): 691-694
被引量:19
标识
DOI:10.1089/gtmb.2010.0054
摘要
We conclude that these mutations are rare causes of PD in the Eastern Indian population and, therefore, of little help for genetic counseling and diagnostic purposes.
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