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The Heritability of Amyotrophic Lateral Sclerosis in a Clinically Ascertained United States Research Registry
BACKGROUND: The genetic basis of amyotrophic lateral sclerosis (ALS) is not entirely clear. While there are families with rare highly penetrant mutations in Cu/Zn superoxide dismutase 1 and several other genes that cause apparent Mendelian inheritance of the disease, most ALS occurs in families with...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2011
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3222666/ https://ncbi.nlm.nih.gov/pubmed/22132186 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0027985 |
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