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Epidemiology of cardiomyopathy - A clinical and genetic study of hypertrophic cardiomyopathy: The EPOCH-H study

Biswas Amitabh, Das Soumi, Kapoor Mitali, Seth Sandeep, Bhargava Balram, Rao Vadlamudi Raghavendra

Year : 2015| Volume: 1| Issue : 2 | Page no: 143-149

   This article has been cited by
1 D190Y mutation in C-terminal tail region of TNNI3 gene causing severe form of restrictive cardiomyopathy with mild hypertrophy in an Indian patient
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Meta Gene. 2020; : 100777
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2 Co-Existing Subaortic Stenosis in a Patient With Hypertrophic Obstructive Cardiomyopathy: A Rare and Interesting Finding
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3 TNNT2 5?bp deletion, sedentary lifestyle & abdominal adiposity accentuate the phenotypic severity in hypertrophic cardiomyopathy patients
Amitabh Biswas,Mitali Kapoor,Soumi Das,Sandeep Seth,Balram Bhargava,Vadlamudi Raghavendra Rao
Meta Gene. 2019; 20: 100567
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4 Familial Hypertrophic Cardiomyopathy - Identification of cause and risk stratification through exome sequencing
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Gene. 2018; 660: 151
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