A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation-Reference-Cited by-同舟云学术

A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation

Published:2022-04-11 Issue: Volume: Page:
ISSN:0970-1915
Container-title:Indian Journal of Clinical Biochemistry
language:en
Short-container-title:Ind J Clin Biochem

Author:

Kumar Prabodh,Paramasivam Ganesh,Devasia Tom,Prabhu Mukund,Rai Maneesh K.,Prakashini K.,Mallya Sandeep,Reghunathan Dinesh,Megha A.,Nayak Krishnananda,Moka Rajasekhar

Funder

Science and Engineering Research Board

Council of Scientific and Industrial Research, India

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry

Link

https://link.springer.com/content/pdf/10.1007/s12291-022-01036-w.pdf

Reference7 articles.

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2. Elliott P, Anastakis A, Borger MA, et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy. Eur Heart J. 2014;35:2733–79. https://doi.org/10.1093/eurheartj/ehu284.

3. Jongbloed RJ, Marcelis CL, Doevendans PA, et al. Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy. J Am Coll Cardiol. 2003;41:981–6. https://doi.org/10.1016/S0735-1097(02)03005-X.

4. Marian AJ, Braunwald E. Hypertrophic cardiomyopathy. Circ Res. 2017;121:749–70. https://doi.org/10.1161/CIRCRESAHA.117.311059.

5. Redwood C, Robinson P. Alpha-tropomyosin mutations in inherited cardiomyopathies. J Muscle Res Cell Motil. 2013;34:285–94. https://doi.org/10.1007/s10974-013-9358-5.