HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin (Q33576895)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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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HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin (English)
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John C Morris
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Nigel J Cairns
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John S K Kauwe
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Joanne Norton
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John Budde
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Denise Levitch
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Sumi Chakraverty
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Michael Gitcho
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Lisa Taylor-Reinwald
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Shantia Shears
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Maria I Behrens
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Rajka M Liscic
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Anthony L Hinrichs
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P-H Tu
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Javier Armendariz
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1 September 2006
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60
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314-322
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