UBQLN2mutation causing heterogeneous X-linked dominant neurodegeneration-Reference-Cited by-同舟云学术

UBQLN2mutation causing heterogeneous X-linked dominant neurodegeneration

Published:2014-05 Issue:5 Volume:75 Page:793-798
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Fahed Akl C.¹,McDonough Barbara¹²,Gouvion Cynthia M.³,Newell Kathy L.³,Dure Leon S.⁴,Bebin Martina⁴,Bick Alexander G.¹,Seidman Jonathan G.¹,Harter Donald H.⁵,Seidman Christine E.¹²

Affiliation:

1. Department of Genetics; Harvard Medical School; Boston MA

2. Cardiovascular Division and Howard Hughes Medical Institute, Brigham and Women's Hospital; Boston MA

3. Department of Pathology and Laboratory Medicine; University of Kansas Medical Center; Kansas City KS

4. Departments of Neurology and Pediatrics; University of Alabama at Birmingham; Birmingham AL

5. Department of Neurology; School of Medicine and Health Sciences, George Washington University; Washington DC

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.24164/fullpdf

Reference10 articles.

1. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia;Deng;Nature,2011

2. UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis;Daoud;Neurobiol Aging,2012

3. Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients;Dillen;Neurobiol Aging,2013

4. Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia;Gellera;J Neurol Neurosurg Psychiatry,2013

5. Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis;Millecamps;Neurobiol Aging,2012

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