Huntington’s disease: the coming of age

Author:

Pandey Mritunjay,Rajamma UshaORCID

Funder

Department of Higher Education, Government of Kerala

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference189 articles.

1. Adachi Y. and Nakashima K. 1999 Population genetic study of Huntington’s disease-prevalence and founder’s effect in the San-in area, western Japan. Nippon Rinsho. 57, 900–904.

2. Albin R. L., Reiner A., Anderson K. D., Penney J. B. and Young A. B. 1990 Striatal and nigral neuron subpopulations in rigid Huntington’s disease: implications for the functional anatomy of chorea and rigidity-akinesia. Ann. Neurol. 27, 357–365.

3. Albin R. L., Reiner A., Anderson K. D., Dure L. S. 4th, Handelin B., Balfour R. et al. 1992 Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington’s disease. Ann. Neurol. 31, 425–430.

4. Almqvist E. W., Elterman D. S., MacLeod P. M. and Hayden M. R. 2001 High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia. Clin. Genet. 60, 198–205.

5. Andrade M. A. and Bork P. 1995 HEAT repeats in the Huntington’s disease protein. Nat. Genet. 11, 115–116.

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