ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease (Q28219731)

Cloning of two novel ABC transporters mapping on human chromosome 9

Europe PubMed Central

title

ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease (English)

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main subject

Alabama

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coronary artery disease

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Seung Ho Hong

1

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Jeffrey Rhyne

series ordinal

2

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Karen Zeller

series ordinal

3

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Michael Miller

series ordinal

4

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language of work or name

English

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publication date

October 2002

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published in

Atherosclerosis

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volume

164

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issue

2

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page(s)

245-50

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cites work

1 reference

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The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

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Common and rare ABCA1 variants affecting plasma HDL cholesterol

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Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

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Dyslipidemias with desirable plasma total cholesterol levels and angiographically demonstrated coronary artery disease

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The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

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Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations

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