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HTT haplogroups in Finnish patients with Huntington disease

OBJECTIVE: To study genetic causes of the low frequency of Huntington disease (HD) in the Finnish population, we determined HTT haplogroups in the population and patients with HD and analyzed intergenerational Cytosine-Adenosine-Guanosine (CAG) stability. METHODS: A national cohort of patients with...

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Detalles Bibliográficos
Autores principales:	Ylönen, Susanna, Sipilä, Jussi O.T., Hietala, Marja, Majamaa, Kari
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer 2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481225/ https://www.ncbi.nlm.nih.gov/pubmed/31086827 http://dx.doi.org/10.1212/NXG.0000000000000334

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