Latest Channelopathy Stories
19th Annual “The Eyes of Christmas™ ” Television Special for the Visually Impaired Kicks-off with “It’s A Wonderful Life,” Audio Described by former US President George H.W.
A promising technology may enable doctors to diagnose and possibly treat in utero a common cause of stillbirth and sudden death in infants.
Inter-professional Care provided to a 9 year old girl with genetic mutation for Long QT Syndrome. New York (PRWEB) November 08, 2013 As a researcher
LizArt Gallery, a website featuring photographs and gifts from artist Elizabeth Sohnle, is pleased to announce a new campaign aimed to raise awareness and funds for cystic fibrosis.
Announcement comes on the first day of the North American Cystic Fibrosis Conference, where the latest data on N8's patented biopharmaceutical will be presented. Columbus,
Research led by physician-scientists at Bascom Palmer Eye Institute of the University of Miami Miller School of Medicine has produced a breakthrough discovery in diagnosing retinitis pigmentosa, a blinding disease that affects about 1 in 4,000 people in the United States.
Cystic fibrosis, also called mucoviscidosis, is an autosomal recessive genetic disorder of the viscous secretions in the body. In turn, it effects the lungs, pancreas, liver, and intestines, as well as all other exocrine glands in the body. The most common genetic mutation that causes CF is a deletion of three nucleotides that results in a loss of phenylalanine, an amino acid at the 508th position on the protein. It should be noted, however, that there are over a thousand other mutations that...
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