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PMID: 8096434 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis.

Cell ·Vol. 73 ·No. 1 ·1993-04-09 ·Pages 159-68

Curran ME, Atkinson DL, Ewart AK, Morris CA, Leppert MF, Keating MT

Abstract

To identify genes involved in vascular disease, we investigated patients with supravalvular aortic stenosis (SVAS), an inherited vascular disorder that causes hemodynamically significant narrowing of large elastic arteries. Pulsed-field gel and Southern analyses showed that a translocation near the elastin gene cosegregated with SVAS in one family. DNA sequence analyses demonstrated that the translocation disrupted the elastin gene and localized the breakpoint to exon 28. Taken together with our previous study linking SVAS to the elastin gene in two additional families and existing knowledge of vascular biology, these data suggest that mutations in the elastin gene can cause SVAS.

MeSH Terms
Amino Acid Sequence Aortic Valve Stenosis/genetics Base Sequence Chromosome Mapping Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 7 Elastin/genetics Female Genetic Linkage Humans Hybrid Cells Male Molecular Sequence Data Pedigree Polymorphism, Restriction Fragment Length Syndrome Translocation, Genetic
Chemicals
Elastin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Curran M E
Department of Human Genetics, University of Utah, Salt Lake City 84112.
Atkinson D L
Ewart A K
Morris C A
Leppert M F
Keating M T
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1993-04-09
Pages
159-68
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCRR NIH HHS · MO1-RR00064 · United States
NHLBI NIH HHS · R01HL4807 · United States
Databases
GENBANK
L09220, L09221, L09222, L09223, L09224, L09225, L33709, S57887, S63764, S63803
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