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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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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BMJ Group
2010
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2988617/ https://ncbi.nlm.nih.gov/pubmed/20861059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2010.207464 |
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