No abstract available
MeSH terms
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Amyloid Neuropathies, Familial / complications*
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Amyloid Neuropathies, Familial / diagnosis
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Amyloid Neuropathies, Familial / genetics
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Cardiomyopathy, Hypertrophic / diagnosis
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Diagnosis, Differential
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Heart Failure / etiology*
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Humans
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Male
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Middle Aged
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Mutation*
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Prealbumin / genetics*
Substances
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Prealbumin
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TTR protein, human
Supplementary concepts
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Amyloidosis, Hereditary, Transthyretin-Related