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Comment

. 1999 Oct;104(8):1015-7.

doi: 10.1172/JCI8509.

ABC1: connecting yellow tonsils, neuropathy, and very low HDL

H H Hobbs¹, D J Rader

Affiliations

Affiliation

¹ Departments of Internal Medicine and Molecular Genetics, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75229, USA. helen.hobbs@email.swmed.edu

PMID: 10525038
PMCID: PMC408871
DOI: 10.1172/JCI8509

Comment

ABC1: connecting yellow tonsils, neuropathy, and very low HDL

H H Hobbs et al. J Clin Invest. 1999 Oct.

. 1999 Oct;104(8):1015-7.

doi: 10.1172/JCI8509.

Authors

H H Hobbs¹, D J Rader

Affiliation

¹ Departments of Internal Medicine and Molecular Genetics, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75229, USA. helen.hobbs@email.swmed.edu

PMID: 10525038
PMCID: PMC408871
DOI: 10.1172/JCI8509

No abstract available

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Comment on

The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway.
Lawn RM, Wade DP, Garvin MR, Wang X, Schwartz K, Porter JG, Seilhamer JJ, Vaughan AM, Oram JF. Lawn RM, et al. J Clin Invest. 1999 Oct;104(8):R25-31. doi: 10.1172/JCI8119. J Clin Invest. 1999. PMID: 10525055 Free PMC article.

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References

1. Fredrickson DS, Altrocchi PH, Avioli LV, Goodman DS, Goodman HC. Tangier disease: combined clinical staff conference at the National Institutes of Health. 1961;55:1016–1031.
1. Assman, G., von Eckardstein, A., and Brewer, H.B. 1995. Familial high density lipoprotein deficiency: Tangier disease. In The metabolic and molecular bases of inherited disease. C.R. Scriver, A.L. Beaudet, and W.S. Sly, editors. McGraw-Hill. New York, NY. 2053–2072.
1. Bodzioch M, et al. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat Genet. 1999;22:347–351. - PubMed
1. Rust S, et al. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet. 1999;22:352–355. - PubMed
1. Brooks-Wilson A, et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet. 1999;22:336–345. - PubMed

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