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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
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
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
Huntingtons Disease Etiology | Medically Roche Researchers identified that the number of CAG trinucleotide repeat expansions in the huntingtin gene (HTT) has been shown to correlate with the age of disease onset 2,3 It is known that a CAG repeat length of ≥40 results in definite HD, 1,7-10 CAG repeat length inversely correlates with age of onset, 3,7 and other genetic and environmental
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