No abstract available
MeSH terms
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Chromogranins
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Chromosome Disorders / genetics
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Fibrous Dysplasia, Polyostotic / genetics
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GTP-Binding Protein alpha Subunits, Gs / genetics
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Genetic Diseases, Inborn / genetics*
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Humans
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Huntington Disease / genetics
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Mosaicism*
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Mutation
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Neurofibromatoses / genetics
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Osteogenesis Imperfecta / genetics
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Trinucleotide Repeats / genetics
Substances
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Chromogranins
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GNAS protein, human
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GTP-Binding Protein alpha Subunits, Gs