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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

✍ Scribed by Odity Mukherjee; Pau Pastor; Nigel J. Cairns; Sumi Chakraverty; John S. K. Kauwe; Shantia Shears; Maria I. Behrens; John Budde; Anthony L. Hinrichs; Joanne Norton; Denise Levitch; Lisa Taylor-Reinwald; Michael Gitcho; P.-H. Tu; Lea Tenenholz Grinberg; Rajka M. Liscic; Javier Armendariz; John C. Morris; Alison M. Goate


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
800 KB
Volume
60
Category
Article
ISSN
0364-5134

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