No abstract available
MeSH terms
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Amino Acid Substitution
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Autistic Disorder* / genetics
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Autistic Disorder* / physiopathology
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Calcium Channels, L-Type / genetics*
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Child
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Electrocardiography*
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Gain of Function Mutation*
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Humans
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Long QT Syndrome* / genetics
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Long QT Syndrome* / physiopathology
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Male
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Mutation, Missense*
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Syndactyly* / genetics
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Syndactyly* / physiopathology
Substances
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CACNA1C protein, human
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Calcium Channels, L-Type