Genetic Counseling in Huntington's Disease: Potential New Challenges on Horizon?

Huntington's disease (HD) is a rare, hereditary, neurodegenerative and dominantly transmitted disorder affecting about 10 out of 100,000 people in Western Countries. The genetic cause is a CAG repeat expansion in the huntingtin gene (HTT), which is unstable and may further increase its length i...

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Detalles Bibliográficos
Autores principales: Migliore, Simone, Jankovic, Joseph, Squitieri, Ferdinando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503085/
https://www.ncbi.nlm.nih.gov/pubmed/31114543
http://dx.doi.org/10.3389/fneur.2019.00453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503085/
https://www.ncbi.nlm.nih.gov/pubmed/31114543
http://dx.doi.org/10.3389/fneur.2019.00453

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