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Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative

Author:

Rosa Rademakers,Matt Baker,Jennifer Gass,Jennifer Adamson,Edward D Huey,Parastoo Momeni,Salvatore Spina,Giovanni Coppola,Anna M Karydas,Heather Stewart,Nancy Johnson,Ging-Yuek Hsiung,Brendan Kelley,Karen Kuntz,Ellen Steinbart,Elisabeth McCarty Wood et al.

Publication:

The Lancet Neurology

Publisher:

Elsevier

Date:

October 2007

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