Multisystem proteinopathy: Table
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference33 articles.
1. Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone
2. Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia
3. Mutational analysis of the VCP gene in Parkinson's disease
4. A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease
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1. Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1;Neurology Genetics;2024-10
2. Defining the landscape of TIA1 and SQSTM1 digenic myopathy;Neuromuscular Disorders;2024-09
3. Physiological functions of ULK1/2;Journal of Molecular Biology;2024-08
4. Analysis of clinical and gene mutation characteristics in patients of isolated myopathy caused by <italic>HNRNPA1</italic> mutation;SCIENTIA SINICA Vitae;2024-08-01
5. Dominant stop‐loss HNRNPA1 variants in juvenile‐onset myopathy;Muscle & Nerve;2024-07-28
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