Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease

Author:

Li X.‐Y.1,Li H.‐L.1,Dong Y.1,Gao B.1,Cheng H.‐R.1,Ni W.1,Gan S.‐R.2,Liu Z.‐J.3,Burgunder J.‐M.4ORCID,Wu Z.‐Y.156ORCID

Affiliation:

1. Department of Neurology and Research Center of Neurology in Second Affiliated Hospital and Key Laboratory of Medical Neurobiology of Zhejiang Province Zhejiang University School of Medicine HangzhouChina

2. Department of Neurology and Institute of Neurology First Affiliated Hospital Fujian Medical University FuzhouChina

3. Department of Neurology and Institute of Neurology Huashan Hospital Shanghai Medical College Fudan University Shanghai China

4. Swiss Huntington’s Disease Centre, Siloah, Gümligen and Department of Neurology, University of Bern Bern Switzerland

5. Joint Institute for Genetics and Genome Medicine between Zhejiang University and University of Toronto Zhejiang University HangzhouChina

6. CAS Center for Excellence in Brain Science and Intelligence Technology Shanghai China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference23 articles.

1. A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats

2. Huntington's disease

3. Huntington disease: genetics and epidemiology;Conneally PM;Am J Hum Genet,1984

4. Epidemiological and Genetic Studies of Huntington's Disease in the San-in Area of Japan

5. Huntington's disease in Hong Kong Chinese: epidemiology and clinical picture;Chang CM;Clin Exp Neurol,1994

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