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LGMD2
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Skeletal muscle psoas
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Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1.
The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3-related muscular dystrop…
Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb-Girdel Muscular Dys…
CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related.
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-…
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A Study to Evaluate the Safety of LION-101 in Subjects With Genetic Confirmation of LGMD2I/R9 (Part1…
Device for Breathing Frequency Monitoring in Muscular Dystrophy
Pilot Study of Cardiac MR in Patients With Muscular Dystrophy
Heart Imaging in Children With Muscular Dystrophy
Congenital Muscle Disease Study of Patient and Family Reported Medical Information
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