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Hereditary hemorrhagic telangiectasia - Symptoms and causes HHT is a condition of gene changes, called genetic, that you get from your parents It is an autosomal dominant disorder That means if one of your parents has HHT, you have a 50% chance of getting it If you have HHT, each of your children has a 50% chance of getting it from you
Huntingtin - Wikipedia The Huntingtin (HTT) protein is a large, predominantly α-helical molecule composed of 3,144 amino acids and weighing approximately 348kDa in its canonical form
HTT Gene - GeneCards | HD Protein | HD Antibody HTT (Huntingtin) is a Protein Coding gene Diseases associated with HTT include Huntington Disease and Lopes-Maciel-Rodan Syndrome Among its related pathways are Gene expression (Transcription) and Transcriptional Regulation by MECP2
Huntington Disease | Learn Science at Scitable - Nature Today, researchers can literally "measure" the HD-associated gene, called huntingtin (HTT), by determining the number of repeats of a set of three specific bases within this gene
Genentech: Huntingtons Disease HD is a rare, fatal, genetic disease that causes the breakdown of nerve cells in the brain over time HD affects a person’s mental, behavioral and physical abilities, including their ability to reason, walk and speak 1 Who is affected by HD?