Items related to Troponin Sequence Variation in Health and Disease

Troponin Sequence Variation in Health and Disease - Softcover

 
9786200265678: Troponin Sequence Variation in Health and Disease

Synopsis

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.

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  • PublisherLAP LAMBERT Academic Publishing
  • Publication date2019
  • ISBN 10 6200265674
  • ISBN 13 9786200265678
  • BindingPaperback
  • LanguageEnglish
  • Number of pages88

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Singla, Sonia
Published by LAP LAMBERT Academic Publishing, 2019
ISBN 10: 6200265674 ISBN 13: 9786200265678
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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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. 88 pp. Englisch. Seller Inventory # 9786200265678

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Singla, Sonia
Published by LAP LAMBERT Academic Publishing, 2019
ISBN 10: 6200265674 ISBN 13: 9786200265678
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Sonia Singla
Published by LAP LAMBERT Academic Publishing, 2019
ISBN 10: 6200265674 ISBN 13: 9786200265678
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Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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. Seller Inventory # 9786200265678

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Singla, Sonia
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Sonia Singla
Published by LAP LAMBERT Academic Publishing, 2019
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Singla SoniaSonia 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. Seller Inventory # 385886729

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