Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2004.00755.x/fullpdf
Reference20 articles.
1. Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development
2. Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
3. Dynamic Interactions of Behavior and Amine Neurochemistry in Acquisition and Maintenance of Social Rank in Crayfish
4. Defective membrane repair in dysferlin-deficient muscular dystrophy
5. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
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1. A Novel Homozygous Variant in DYSF Gene Is Associated with Autosomal Recessive Limb Girdle Muscular Dystrophy R2/2B;International Journal of Molecular Sciences;2022-08-11
2. Over three decades of natural history of limb girdle muscular dystrophy type R1/2A and R2/2B: Mathematical modelling of a multifactorial study;Neuromuscular Disorders;2021-06
3. Multiple acyl-coenzyme A dehydrogenase deficiency shows a possible founder effect and is the most frequent cause of lipid storage myopathy in Iran;Journal of the Neurological Sciences;2020-04
4. Antisense-Mediated Skipping of Dysferlin Exons in Control and Dysferlinopathy Patient-Derived Cells;Nucleic Acid Therapeutics;2020-04-01
5. Twenty-Year Clinical Progression of Dysferlinopathy in Patients from Dagestan;Frontiers in Neurology;2017-03-08
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