Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree.
Clin Case Rep
| Authors | |
| 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. |
| Year of Publication | 2016
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| Journal | Clin Case Rep
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| Volume | 4
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| Issue | 12
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| Pages | 1191-1194
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| Date Published | 2016 Dec
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| DOI | 10.1002/ccr3.743
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| PubMed ID | 27980761
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| PubMed Central ID | PMC5134195
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| Links |