A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)
| Data(s) |
01/02/2012
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| Resumo |
To further characterize the neuropathology of the heterogeneous molecular disorder frontotemporal lobar degeneration (FTLD) with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy (FTLD-TDP). |
| Formato |
application/pdf |
| Identificador |
http://eprints.aston.ac.uk/16166/1/FTLD_TDP_density_Missouri_R2.pdf Armstrong, Richard A.; Carter, D. and Cairns, N.J. (2012). A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP). Neuropathology and Applied Neurobiology, 38 (1), pp. 25-38. |
| Relação |
http://eprints.aston.ac.uk/16166/ |
| Tipo |
Article PeerReviewed |
