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Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS)

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a progressive lethal disorder of large motor neurons of the spinal cord and brain. In approximately 20% of the familial and 2% of sporadic cases the disease is due to a defect in the gene encoding the cytosolic antioxidant enzyme Cu, Zn-superoxide d...

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Detalhes bibliográficos
Main Authors: Silahtaroglu, Asli N, Brondum-Nielsen, Karen, Gredal, Ole, Werdelin, Lene, Panas, Marios, Petersen, Michael B, Tommerup, Niels, Tümer, Zeynep
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2002
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC107843/
https://ncbi.nlm.nih.gov/pubmed/11991808
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-3-5
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