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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134195/
https://www.ncbi.nlm.nih.gov/pubmed/27980761
http://dx.doi.org/10.1002/ccr3.743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134195/
https://www.ncbi.nlm.nih.gov/pubmed/27980761
http://dx.doi.org/10.1002/ccr3.743

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