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Article

Transthyretin Val30Met mutation in an African American with cardiac amyloidosis.

Congestive heart failure (Greenwich, Conn.) - 1 Jan 2000

Schulze P Christian, Maurer Mathew S

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Share to Amyloidosis
Share to Echocardiography
Share to Heart Diseases
Share to Hypertrophy, Left Ventricular

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 20412473
DOI: 10.1111/j.1751-7133.2009.00122.x
PMCID: PMC4938000

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Transthyretin Val30Met mutation in an African American with cardiac amyloidosis.PMID 20412473Read ↗

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Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.Semantic proximity Read ↗

Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant.Semantic proximity Read ↗

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Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.Semantic proximity Read ↗

Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy.Semantic proximity Read ↗

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