CHMP2B C-truncating mutations in frontotemporal lobar...

Human Molecular Genetics 2007 / 10 Vol. 17; Iss. 2

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

van der Zee, J., Urwin, H., Engelborghs, S., Bruyland, M., Vandenberghe, R., Dermaut, B., De Pooter, T., Peeters, K., Santens, P., De Deyn, P. P., Fisher, E. M., Collinge, J., Isaacs, A. M., Van Broec
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Volume:
17
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddm309
Date:
October, 2007
File:
PDF, 581 KB
english, 2007
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