A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family-Reference-Cited by-同舟云学术

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A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family

Published:2013-01 Issue:1 Volume:52 Page:9-16
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Gu Jie-Mei,Ke Yao-Hua,Yue Hua,Liu Yu-Juan,Zhang Zeng,Zhang Hao,Hu Wei-Wei,Wang Chun,He Jin-Wei,Hu Yun-Qiu,Li Miao,Fu Wen-Zhen,Zhang Zhen-Lin

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Shanghai Rising-Star Program

Academic Leaders in Health Sciences in Shanghai

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. A new familial disorder of combined lower motor neuron degeneration and skeletal disorganization;Tucker;Trans Assoc Am Physicians,1982

2. Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia;Weihl;Neuromuscul Disord,2009

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

4. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy;Guinto;Acta Neuropathol,2007

5. Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family;Kim;Arch Neurol,2011

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4. Clinical Characteristics and Pathogenic Gene Identification in Chinese Patients With Paget’s Disease of Bone;Frontiers in Endocrinology;2022-03-09

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