Program in Molecular Medicine
Nervous System Diseases
Atypical manifestation of Huntington's disease (HD) could inform ongoing research into HD genetic modifiers not present in the primarily European populations studied to date. This work demonstrates that expanding HD genetic testing into under-resourced healthcare settings can benefit both local communities and ongoing research into HD etiology and new therapies.
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Copyright © 2016 The Authors. Citation: Clin Case Rep. 2016 Nov 11;4(12):1191-1194. eCollection 2016 Dec. Link to article on publisher's site
DOI of Published Version
Atypical clinical features, Bangladeshi family tree, CAG repeat, Huntington's disease, mutation
Clinical case reports
Al-Mamun, Md Mahfuz; Sarker, Suprovath Kumar; Qadri, Syeda Kashfi; Shirin, Tahmina; Mohammad, Quazi Deen; LaRocque, Regina; Karlsson, Elinor K.; Saha, Narayan; Asaduzzaman, Muhammad; Qadri, Firdausi; and Mannoor, Md Kaiissar, "Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree" (2016). Open Access Articles. 2993.
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.