Φορτώνει......
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia
AIMS: Frontotemporal lobar degeneration (FTLD) is a progressive neurodegenerative disease and is the second most common form of young onset dementia after Alzheimer's disease (AD). An autosomal dominant pattern of inheritance is present in around 25–50% of FTLD cases indicating a strong genetic...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neuropathol Appl Neurobiol |
|---|---|
| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BlackWell Publishing Ltd
2014
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4260146/ https://ncbi.nlm.nih.gov/pubmed/24286341 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nan.12100 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|