The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot (vol 171, pg 925, 2016)

被引:3
作者
Mata, Ignacio F. [1 ]
Davis, Marie Y. [1 ]
Lopez, Alexis N. [1 ]
Dorschner, Michael O. [1 ]
Martinez, Erica [1 ]
Yearout, Dora [1 ]
Cholerton, Brenna A. [1 ]
Hu, Shu-Ching [1 ]
Edwards, Karen L. [1 ]
Bird, Thomas D. [1 ]
Zabetian, Cyrus P. [1 ]
机构
[1] VA Puget Sound Hlth Care Syst, GRECC S-182,1660 South Columbian Way, Seattle, WA 98108 USA
关键词
D O I
10.1002/ajmg.b.32510
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:113 / 113
页数:1
相关论文
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[1]   The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot (vol 171, pg 925, 2016) [J].
Mata, Ignacio F. ;
Davis, Marie Y. ;
Lopez, Alexis N. ;
Dorschner, Michael O. ;
Martinez, Erica ;
Yearout, Dora ;
Cholerton, Brenna A. ;
Hu, Shu-Ching ;
Edwards, Karen L. ;
Bird, Thomas D. ;
Zabetian, Cyrus P. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2017, 174 (01) :113-113
[2]   The Discovery of LRRK2 p.R1441S, a Novel Mutation for Parkinson's Disease, Adds to the Complexity of a Mutational Hotspot [J].
Mata, Ignacio F. ;
Davis, Marie Y. ;
Lopez, Alexis N. ;
Dorschner, Michael O. ;
Martinez, Erica ;
Yearout, Dora ;
Cholerton, Brenna A. ;
Hu, Shu-Ching ;
Edwards, Karen L. ;
Bird, Thomas D. ;
Zabetian, Cyrus P. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2016, 171 (07) :925-930