An estimate of amyotrophic lateral sclerosis heritability using twin data

BACKGROUND: Causative gene mutations have been identified in about 2% of those with amyotrophic lateral sclerosis (ALS), often, but not always, when there is a strong family history. There is an assumption that there is a genetic component to all ALS, but genome-wide association studies have yet to...

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Detalles Bibliográficos
Autores principales: Al-Chalabi, A, Fang, F, Hanby, M F, Leigh, P N, Shaw, C E, Ye, W, Rijsdijk, F
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2010
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988617/
https://www.ncbi.nlm.nih.gov/pubmed/20861059
http://dx.doi.org/10.1136/jnnp.2010.207464

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988617/
https://www.ncbi.nlm.nih.gov/pubmed/20861059
http://dx.doi.org/10.1136/jnnp.2010.207464

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