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Gene's mutations found to cause life-threatening aortic disease

's team continues to scrutinize a stretch of chromosome 5 to pinpoint another genetic variation that they earlier mapped to that area of the genome. Researchers elsewhere have mapped two other genetic variations affecting single families to chromosomes 11 and 16.

Milewicz also is on the faculty of the UT Graduate School of Biomedical Sciences at Houston and is appointed to the faculty of the Brown Foundation Institute of Molecular Medicine for the Prevention of Human Diseases (IMM).


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Contact: Scott Merville
scott.merville@uth.tmc.edu
713-500-3042
University of Texas Health Science Center at Houston
22-Jul-2005


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