Nonsynonymous Variants in MC1R Are Rare in Chinese Parkinson Disease Cases Reply

被引：1
作者：
Tell-Marti, Gemma [1 ,2 ,3 ]
Anton Puig-Butille, Joan [2 ,3 ,4 ]
Potrony, Miriam [1 ,2 ]
Badenas, Celia [2 ,3 ,4 ]
Mila, Montserrat [2 ,3 ,4 ]
Malvehy, Josep [1 ,2 ,3 ]
Jose Marti, Maria [5 ]
Ezquerra, Mario [5 ]
Fernandez-Santiago, Ruben [5 ]
Puig, Susana [1 ,2 ,3 ,6 ]
机构：
[1] Hosp Clin Barcelona, Dept Dermatol, Melanoma Unit, Barcelona, Spain
[2] August Pi & Sunyer Biomed Res Inst IDIBAPS, Barcelona, Spain
[3] Carlos III Hlth Inst ISCIII, Ctr Networked Biomed Res Rare Dis CIBERER, Barcelona, Spain
[4] Hosp Clin Barcelona, Biochem & Mol Genet Serv, Barcelona, Spain
[5] Hosp Clin Barcelona, Ctr Networked Biomed Res Neurodegenerat Dis CIBER, August Pi & Sunyer Biomed Res Inst IDIBAPS, Dept Clin & Expt Neurol,Lab Neurodegenerat Disord, Barcelona, Spain
[6] Univ Barcelona, Dept Med, Barcelona, Spain
来源：
ANNALS OF NEUROLOGY | 2015年 / 78卷 / 01期
关键词：
LRRK2; G2019S; HAIR COLOR; MELANOMA; GENE; POPULATION; PHENOTYPE; MUTATIONS; RISK;
D O I：
10.1002/ana.24418
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：153 / 154
页数：2
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