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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 9, 2023. (Total: 223907Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hypertrophy and MYL2[original query]
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
European journal of human genetics : EJHG 2002 Nov 10 (11): 741-8.
Kabaeva Zhyldyz T, Perrot Andreas, Wolter Bastian, Dietz Rainer, Cardim Nuno, Correia João Martins, Schulte Hagen D, Aldashev Almaz A, Mirrakhimov Mirsaid M, Osterziel Karl Jos
Shared genetic causes of cardiac hypertrophy in children and adults.
The New England journal of medicine 2008 May 358 (18): 1899-908.
Morita Hiroyuki, Rehm Heidi L, Menesses Andres, McDonough Barbara, Roberts Amy E, Kucherlapati Raju, Towbin Jeffrey A, Seidman J G, Seidman Christine
Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
DNA and cell biology 2015 May 34 (5): 350-9.
Selvi Rani Deepa, Nallari Pratibha, Dhandapany Perundurai S, Rani Jhansi, Meraj Khunza, Ganesan Mala, Narasimhan Calambur, Thangaraj Kumarasa
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