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dc.contributor.authorAl-Mamun, Md Mahfuz
dc.contributor.authorSarker, Suprovath Kumar
dc.contributor.authorQadri, Syeda Kashfi
dc.contributor.authorShirin, Tahmina
dc.contributor.authorMohammad, Quazi Deen
dc.contributor.authorLaRocque, Regina
dc.contributor.authorKarlsson, Elinor K
dc.contributor.authorSaha, Narayan
dc.contributor.authorAsaduzzaman, Muhammad
dc.contributor.authorQadri, Firdausi
dc.contributor.authorMannoor, Md Kaiissar
dc.date2022-08-11T08:09:46.000
dc.date.accessioned2022-08-23T16:42:57Z
dc.date.available2022-08-23T16:42:57Z
dc.date.issued2016-11-11
dc.date.submitted2017-04-14
dc.identifier.citationClin Case Rep. 2016 Nov 11;4(12):1191-1194. eCollection 2016 Dec. <a href="https://doi.org/10.1002/ccr3.743">Link to article on publisher's site</a>
dc.identifier.issn2050-0904 (Linking)
dc.identifier.doi10.1002/ccr3.743
dc.identifier.pmid27980761
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40195
dc.description.abstractAtypical 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27980761&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsCopyright © 2016 The Authors.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAtypical clinical features
dc.subjectBangladeshi family tree
dc.subjectCAG repeat
dc.subjectHuntington's disease
dc.subjectmutation
dc.subjectNervous System Diseases
dc.titleExamination of Huntington's disease with atypical clinical features in a Bangladeshi family tree
dc.typeJournal Article
dc.source.journaltitleClinical case reports
dc.source.volume4
dc.source.issue12
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3998&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2993
dc.identifier.contextkey10021732
refterms.dateFOA2022-08-23T16:42:57Z
html.description.abstract<p>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.</p>
dc.identifier.submissionpathoapubs/2993
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages1191-1194


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Copyright © 2016 The Authors.
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