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Coalition to Cure Calpain 3 (C3) is pleased to announce the publication of important research undertaken by Dr. Rita Perlingeiro, Professor of Medicine, University of Minnesota, and colleagues.The paper, titled “Gene Correction of LGMD2A Specific iPSCs for the Development of Targeted Autologous Cell Therapy,” was published in.
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Calpainopathy Calpainopathy Starling, Alessandra; Paula, Flavia; Silva, Helga; Vainzof, Mariz; Zatz, Mayana 2007-06-02 00:00:00 Five affected siblings were referred with a probable diagnosis of proximal adult-type spinal muscular atro- phy (SMA) based on lower motor neuron signs (muscle weakness and atrophy, hypotony, hypoactive or absent reflexes, and fasciculations), normal or borderline.
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The Russian literature gives inadequate attention to the problem of one of the most common form of autosomal recessive progressive limb-girdle muscular dystrophies type 2A (LGMD2A) (calpainopathy).
Limb-girdle muscular dystrophy (LGMD) 2A (calpainopathy) is the most frequent form of LGMD in many European countries. The increasing demand for a molecular diagnosis makes the identification of.
Limb girdle muscular dystrophies (LGMD) are a heterogeneous group of genetic disorders characterised by progressive weakness of the pelvic and shoulder girdle muscles and a great variability in.
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