G. Michael Felker, M.D http://genericcialishelp.com/faq ., M.H.S., Kerry L. Lee, Ph.D., David A. Bull, M.D., Margaret M. Redfield, M.D., Lynne W. Stevenson, M.D., Steven R. Goldsmith, M.D., Martin M. LeWinter, M.D., Anita Deswal, M.D., M.P.H., Jean L. Rouleau, M.D., Elizabeth O. Ofili, M.D., M.P.H., Kevin J. Anstrom, Ph.D., Adrian F. Hernandez, M.D., Steven E. McNulty, M.S., Eric J. Velazquez, M.D., Abdallah G. Kfoury, M.D., Horng H. Chen, M.B., B.Ch., Michael M. Givertz, M.D., Marc J. Semigran, M.D., Bradley A. Bart, M.D., Alice M. Mascette, M.D., Eugene Braunwald, M.D., and Christopher M.
In addition, the estimates of frequency and penetrance for the condition allele recommend that the disease models for familial interstitial pneumonia and idiopathic pulmonary fibrosis are related. The chances ratio for disease among subjects who were heterozygous and those who were homozygous for the rarer allele of this SNP were 6.8 and 20.8 , respectively, for familial interstitial pneumonia, and 9.0 and 21.8 , respectively, for idiopathic pulmonary fibrosis . To be certain that this SNP was not tagging another SNP in the MUC5B promoter region, we resequenced the 4-kb region upstream of the MUC5B transcription begin site in 48 subjects with idiopathic pulmonary fibrosis and 48 controls .