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A functionally significant polymorphism in ID3 is associated with human coronary pathology.
AIMS:We previously identified association between the ID3 SNP rs11574 and carotid intima-media thickness in the Diabetes Heart Study, a predominantly White diabetic population. The nonsynonymous SNP rs11574 results in an amino acid substitution in the C-terminal region of ID3, attenuating the domina...
Tallennettuna:
Päätekijät: | , , , , , , , , , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
Public Library of Science (PLoS)
2014-01-01
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Sarja: | PLoS ONE |
Linkit: | http://europepmc.org/articles/PMC3946163?pdf=render |
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