transient receptor potential cation channel subfamily M member 4
OMIM: 606936, Gene2Phenotype
Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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TRPM4 in Progressive cardiac conduction disease
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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Phenotypes
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TRPM4 in Short QT syndrome
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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TRPM4 in Brugada syndrome and cardiac sodium channel disease
Level 3: Cardiac arrhythmia
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review | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
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Phenotypes
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TRPM4 in Severe Paediatric Disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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