LAMP-2B regulates human cardiomyocyte function by mediating autophagosome–lysosome fusion | PNAS
LAMP-2B regulates human cardiomyocyte function by mediating autophagosome–lysosome fusion | PNAS
Epigenetic gene expression links heart failure to memory impairment | EMBO Molecular Medicine
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![PDF] A phenocopy of sarcomeric hypertrophic cardiomyopathy: LAMP2 cardiomyopathy (Danon disease) from China. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/95cb1dd3fd02bd913a834785d8f0c09bdc983dfb/2-Figure2-1.png "PDF] A phenocopy of sarcomeric hypertrophic cardiomyopathy: LAMP2 cardiomyopathy (Danon disease) from China. | Semantic Scholar")
PDF] A phenocopy of sarcomeric hypertrophic cardiomyopathy: LAMP2 cardiomyopathy (Danon disease) from China. | Semantic Scholar
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LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart | Journal of the American Heart Association
LAMP-2B regulates human cardiomyocyte function by mediating autophagosome–lysosome fusion | PNAS
LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart | Journal of the American Heart Association
Towards precision medicine in heart failure | Nature Reviews Cardiology
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LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart | Journal of the American Heart Association
A family with Danon disease caused by a splice site mutation in LAMP2 that generates a truncated protein - Zhou - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart | Journal of the American Heart Association
Role of the Epigenome in Heart Failure | Physiological Reviews
IJMS | Free Full-Text | A Nationwide Survey on Danon Disease in Japan
Small-Vessel Vasculopathy Due to Aberrant Autophagy in LAMP-2 Deficiency | Scientific Reports
A novel truncating variant in the LAMP2 gene in a young woman with hypertrophic cardiomyopathy and variable clinical course in the family
Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy | NEJM
Impaired autophagy: The collateral damage of lysosomal storage disorders - eBioMedicine
PDF) Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
2022 ACC/AHA/HFSA Guideline for the Management of Heart Failure - Journal of Cardiac Failure
Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review | Journal of the American College of Cardiology
Identification of MYLK3 mutations in familial dilated cardiomyopathy | Scientific Reports
![PDF] A phenocopy of sarcomeric hypertrophic cardiomyopathy: LAMP2 cardiomyopathy (Danon disease) from China. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/95cb1dd3fd02bd913a834785d8f0c09bdc983dfb/2-Figure1-1.png "PDF] A phenocopy of sarcomeric hypertrophic cardiomyopathy: LAMP2 cardiomyopathy (Danon disease) from China. | Semantic Scholar")