Molecular evaluation of human Ubiquilin 2 gene PXX domain in familial frontotemporal dementia patients-Reference-Cited by-同舟云学术

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Molecular evaluation of human Ubiquilin 2 gene PXX domain in familial frontotemporal dementia patients

Published:2012-06-24 Issue:11 Volume:259 Page:2488-2490
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Hernández Isabel,Espinosa Anna,Real Luis Miguel,Galán Jose Jorge,Mauleón Ana,Roca Maiteé Rosende,Tárraga Lluís,Ruiz Agustín,Boada Mercè

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-012-6568-5.pdf

Reference17 articles.

1. Pinsky L, Finlayson MH, Libman I, Scott BH (1975) Familial amyotrophic lateral sclerosis with dementia: a second Canadian family. Clin Genet 7:186–191

2. Robertson EE (1953) Progressive bulbar paralysis showing heredofamilial incidence and intellectual impairment. AMA Arch Neurol Psychiatry 69:196–207

3. Fecto F, Siddique T (2011) SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis. Ann Neurol 70:867–870

4. Ito D, Suzuki N (2011) Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS. Neurology 77:1636–1643

5. DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, Nicholson AM, Finch NA, Flynn H, Adamson J et al (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245–256

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1. Frontotemporal Lobar Degeneration (FTLD): Review and Update for Clinical Neurologists;Current Alzheimer Research;2018-04-05

2. Association of TMEM106B rs1990622 Marker and Frontotemporal Dementia: Evidence for a Recessive Effect and Meta-Analysis;Journal of Alzheimer's Disease;2014-10-30

3. Protein aggregation in amyotrophic lateral sclerosis;Acta Neuropathologica;2013-05-15

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