Huntington Disease: The 'typical' phenotype for the commonest CAG repeat expansion in the ENROLL-HD study across varying functional levels

被引:0
作者
Chang, Florence Ching-Fen [1 ,2 ]
McCusker, Elizabeth [1 ,2 ]
Loy, Clement [1 ,3 ,4 ]
机构
[1] Westmead Hosp, Neurol Dept, Huntington Dis Serv, Sydney, NSW, Australia
[2] Sydney Med Sch, Sydney, NSW, Australia
[3] Univ Sydney, Sch Publ Hlth, Sydney, NSW, Australia
[4] Garvan Inst Med Res, Sydney, NSW, Australia
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P4.039
引用
收藏
页数:2
相关论文
共 32 条
[31]   A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington’s Disease Symptoms [J].
Pratiksha Chheda ;
Milind Chanekar ;
Yogita Salunkhe ;
Tavisha Dama ;
Anurita Pais ;
Shailesh Pande ;
Rajesh Bendre ;
Nilesh Shah .
Molecular Diagnosis & Therapy, 2018, 22 :353-359
[32]   A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms [J].
Chheda, Pratiksha ;
Chanekar, Milind ;
Salunkhe, Yogita ;
Dama, Tavisha ;
Pais, Anurita ;
Pande, Shailesh ;
Bendre, Rajesh ;
Shah, Nilesh .
MOLECULAR DIAGNOSIS & THERAPY, 2018, 22 (03) :353-359