No abstract available
Publication types
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Letter
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Research Support, Non-U.S. Gov't
MeSH terms
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Cardiomyopathy, Hypertrophic / genetics*
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Female
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Genetic Variation
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Glycogen Storage Disease Type IIb / diagnosis
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Glycogen Storage Disease Type IIb / genetics*
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High-Throughput Nucleotide Sequencing
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Humans
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Inheritance Patterns
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Loss of Function Mutation
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Lysosomal-Associated Membrane Protein 2 / genetics*
Substances
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LAMP2 protein, human
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Lysosomal-Associated Membrane Protein 2