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Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
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
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
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UMass Chan Affiliations
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Journal Article
Publication Date
2016-11-11
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Abstract
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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Clin Case Rep. 2016 Nov 11;4(12):1191-1194. eCollection 2016 Dec. Link to article on publisher's site
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DOI
10.1002/ccr3.743
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PubMed ID
27980761
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Copyright © 2016 The Authors.