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A New Familial Amyotrophic Lateral Sclerosis Locus on Chromosome 16q12.1-16q12.2
Familial amyotrophic lateral sclerosis (FALS) affects 5%–10% of cases of amyotrophic lateral sclerosis (ALS) and is inherited as an autosomal dominant condition with incomplete penetrance. One-fifth of these cases of FALS are associated with mutations in copper/zinc-dependent superoxide dismutase (S...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The American Society of Human Genetics
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1180375/ https://ncbi.nlm.nih.gov/pubmed/12830400 |
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