Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK-Reference-Cited by-同舟云学术

Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK

Published:2015-06-23 Issue:6 Volume:87 Page:680-681
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Figueroa-Bonaparte S,Hudson J,Barresi R,Polvikoski T,Williams T,Töpf A,Harris E,Hilton-Jones D,Petty R,Willis T A,Longman C,Dougan C F,Parton M J,Hanna M G,Quinlivan R,Farrugia M E,Guglieri M,Bushby K,Straub V,Lochmüller H,Evangelista T

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference4 articles.

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2. Exome sequencing reveals VCP mutations as a cause of familial ALS;Johnson;Neuron,2010

3. Genotype-phenotype studies of VCP associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia;Mehta;Clin Genet,2013

4. Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree;Miller;J Neurol Neurosurg Psychiatry,2009

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