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Progranulin mutation analysis: Identification of one novel mutation in exon 12 associated with frontotemporal dementia
Progranulin (PGRN) mutations account for an average of 15% of familial FTD cases and 20% of total FTD cases worldwide. Here we investigated the frequency of PGRN mutations in FTD patients (n=116) from a clinical cohort of South India and detected one novel mutation located on exon 12 in a familial b...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neurobiol Aging |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4775422/ https://ncbi.nlm.nih.gov/pubmed/26724960 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2015.11.026 |
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