Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype-Reference-Cited by-同舟云学术

Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype

Published:2012-12 Issue:12 Volume:33 Page:2949.e13-2949.e17
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Synofzik Matthis,Maetzler Walter,Grehl Torsten,Prudlo Johannes,vom Hagen Jennifer Müller,Haack Tobias,Rebassoo Piret,Munz Marita,Schöls Ludger,Biskup Saskia

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference13 articles.

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

4. UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia;Fecto;Muscle Nerve,2012

5. X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny;Huynh;Nat. Rev. Genet,2005

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