Left ventricular deformation abnormalities in a patient with calpainopathy-a case from the three-dimensional speckle-tracking echocardiographic magyar-path study
Calpainopathy or limb-girdle muscular dystrophy type 2A (LGMD2A) is the most common type of autosomal recessive limb-girdle muscular dystrophies. The disease is caused by mutations in the CAPN3 gene encoding calpain, a protein involved in muscle membrane remodeling and repair. This paper gives an ov...
Elmentve itt :
| Szerzők: | |
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| Dokumentumtípus: | Cikk |
| Megjelent: |
2017
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| Sorozat: | QUANTITATIVE IMAGING IN MEDICINE AND SURGERY
7 No. 6 |
| doi: | 10.21037/qims.2017.10.09 |
| mtmt: | 3312341 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/15731 |