Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type
Author:
Publisher
Wiley
Subject
Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.1995.tb01030.x/fullpdf
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1. Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology;Human Molecular Genetics;2017-05-29
2. Cytokine genes as potential biomarkers for muscle weakness in OPMD;Human Molecular Genetics;2016-08-09
3. Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy;Neurology;2015-03-06
4. Atrophy, Fibrosis, and Increased PAX7-Positive Cells in Pharyngeal Muscles of Oculopharyngeal Muscular Dystrophy Patients;Journal of Neuropathology & Experimental Neurology;2013-03
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