Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree

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...

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Bibliografski detalji
Izdano u:Clin Case Rep
Glavni autori: 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, Mannoor, Md Kaiissar
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2016
Teme:
Case Reports
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5134195/
https://ncbi.nlm.nih.gov/pubmed/27980761
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.743
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