Novel valosin-containing protein mutations associated with multisystem proteinopathy-Reference-Cited by-同舟云学术

Novel valosin-containing protein mutations associated with multisystem proteinopathy

Published:2018-06 Issue:6 Volume:28 Page:491-501
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Al-Tahan Sejad,Al-Obeidi Ebaa,Yoshioka Hiroshi,Lakatos Anita^ORCID,Weiss Lan^ORCID,Grafe Marjorie,Palmio Johanna,Wicklund Matt,Harati Yadollah,Omizo Molly^ORCID,Udd Bjarne,Kimonis Virginia

Funder

National Institute of Health

Institute of Clinical and Translational Science

University of California

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference70 articles.

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3. Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone;Kimonis;Genet Med,2000

4. Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia;Kimonis;Am J Med Genet A,2008

5. Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family;Palmio;Neuromuscul Disord,2011

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