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Article

Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations.

Arthritis and rheumatism - 1 Apr 2001

Tan F K, Wang N, Kuwana M, Chakraborty R, Bona C A, Milewicz D M, Arnett F C

Abstract excerpt

OBJECTIVE: Previously, we demonstrated with the use of microsatellite markers that a 2-cM haplotype on chromosome 15q containing the fibrillin 1 gene (FBN1) was strongly associated with systemic sclerosis (SSc) in the Choctaw, a population with high SSc prevalence. In this study, all 69 known FBN1 exons were sequenced to ascertain the presence of changes that might show associations with SSc in the Choctaw and...

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Source

Identifiers

PMID: 11315929
DOI: 10.1002/1529-0131(200104)44:4<893::AID-ANR146>3.0.CO;2-3

Genes

FBN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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