HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
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| Description | scientific article |
| Author/s |
author: Sumi Chakraverty Shantia Shears Alison Goate Pau Pastor Michael A Gitcho Rajka M Liscic Lea T Grinberg Denise Levitch Lisa Taylor-Reinwald John P Budde Nigel J Cairns John S K Kauwe Joanne B Norton Maria I. Behrens John C. Morris Odity Mukherjee |
| Publication date | September 1, 2006 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |