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Progressive Amnestic Dementia, Hippocampal Sclerosis, and Mutation in C9ORF72
The most common cause of familial frontotemporal lobar degeneration with TAR DNA-binding protein-43 pathology (FTLD-TDP) has been found to be an expansion of a hexanucleotide repeat (GGGGCC) in a noncoding region of the gene C9ORF72. Hippocampal sclerosis (HpScl) is a common finding in FTLD-TDP. Our...
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| Main Authors: | , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3926101/ https://ncbi.nlm.nih.gov/pubmed/23922030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-013-1161-2 |
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