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HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

scientific article

Author/s

author: Odity Mukherjee, Lea Tenenholz Grinberg, Pau Pastor, Alison Goate, John C. Morris, Nigel J Cairns, John S K Kauwe, Joanne B Norton, John P Budde, Denise Levitch, Sumi Chakraverty, Michael A Gitcho, Lisa Taylor-Reinwald, Shantia Shears, Maria I. Behrens, Rajka M Liscic

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Work details

Publication date
September 1, 2006
- -
Language
English

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