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Late-onset major depression and parkinsonism in heterozygous ATP7B mutation carriers

Sechi, Gianpietro and Cocco, Giovanni Antonio and Errigo, Alessandra and Rosati, Giulio and Deiana, Luca and Agnetti, Virgilio and Paulus, Kai Stephan and Pes, Giovanni Mario (2005) Late-onset major depression and parkinsonism in heterozygous ATP7B mutation carriers. European Journal of Neurology, Vol. 12 (Suppl. 2), p. 270. eISSN 1468-1331. Article.

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DOI: 10.1111/j.1468-1331.2005.01308.x

Abstract

ATP7B gene mutations cause Wilson’s disease (WD) in homozygous and compound heterozygotes, when both alleles of the gene are involved. We are studying if mutations in an ATP7B single allele may confer susceptibility for parkinsonism.

Item Type:Article
ID Code:1496
Status:Published
Refereed:Yes
Uncontrolled Keywords:ATP7B gene mutations, Wilson’s disease, parkinsonism
Subjects:Area 05 - Scienze biologiche > BIO/12 Biochimica clinica e biologia molecolare clinica
Area 06 - Scienze mediche > MED/26 Neurologia
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze biomediche
001 Università di Sassari > 03 Istituti > Clinica neurologica
Publisher:Blackwell Science / Wiley
eISSN:1468-1331
Copyright Holders:© 2005 EFNS
Additional Information:Poster presented at the 9. Congress of the EFNS, Athens, Greece, 17-20 September 2005.
Deposited On:18 Aug 2009 10:05

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