The P448Lneo−🐁model has a knock-in mutation in the FKRP gene & develops skeletal, respiratory, & cardiac muscle disease. Our ECGenie readily quantifies the significant changes in❤️rate & HRV in this & other 🐁 models of muscular dystrophy.
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Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo− mouse model of FKRP-deficient muscular dystrophy #skeletalmuscle @BioMedCentral https://t.co/j2AZIGXcNL
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Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo− mouse model of FKRP-deficient muscular dystrophy @BioMedCentral https://t.co/j2AZIGXcNL
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New #SkeletalMuscle paper: Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo− mouse model of FKRP-deficient muscular dystrophy. https://t.co/gWwUay2VXP