Beschreibung
Single amino acid substitutions can lead to various diseases like Hypertrophic Cardiomyopathy dilated cardiomyopathy and other diseases. Hypertrophic Cardiomyopathy is an autosomal inherited disease in which the condition is being transmitted from one generation to another ,so far no proper treatment is there for these disease and is found to be about one in every five hundred persons, or likely half of the population of United States suffering from these disease. Mutations in that of Tropomyosin, Troponin has been found to be the cause of these disease; although these disease has shown to be have been linked with that of Myosin heavy chain and its binding protein, but we here are concerned with only Troponin and Tropomyosin, how these change might have occurred.
Autorenporträt
Sonia Singla has done MSc in Biotechnology and MSc in Bioinformatics from University of Leicester, U.K. She has published many articles and has reviewed articles. She is interested in Data Analytics, health and disease.
