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Novel missense mutation in Charged Multivesicular body Protein 2B in a patient with Frontotemporal Dementia
Frontotemporal Dementia (FTD) is the second major cause of dementia in persons under the age of 65 after Alzheimer’s disease (AD). FTD is clinically, pathologically and genetically heterogeneous and has been associated with mutations in different genes located on chromosomes 17, 9 and 3. In our stud...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2974047/ https://ncbi.nlm.nih.gov/pubmed/20592581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WAD.0b013e3181df20c7 |
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