Homo sapiens myosin, heavy chain 7, cardiac muscle, beta, mRNA (cDNA c - Nucleotide

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Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respiration. [Proc Natl Acad Sci U S A. 2024]
Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respiration.
Lee S, Vander Roest AS, Blair CA, Kao K, Bremner SB, Childers MC, Pathak D, Heinrich P, Lee D, Chirikian O, et al. Proc Natl Acad Sci U S A. 2024 May 7; 121(19):e2318413121. Epub 2024 Apr 29.
A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy. [Front Biosci (Schol Ed). 2024]
A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy.
Golubenko MV, Pavlyukova EN, Salakhov RR, Makeeva OA, Puzyrev KV, Glotov OS, Puzyrev VP, Nazarenko MS. Front Biosci (Schol Ed). 2024 Feb 23; 16(1):1.
Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry. [Circ Heart Fail. 2024]
Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry.
Earle NJ, Winbo A, Crawford J, Wheeler M, Stiles R, Donoghue T, Stiles MK, Hayes I, Marcondes L, Martin A, et al. Circ Heart Fail. 2024 Mar; 17(3):e010970. Epub 2024 Mar 8.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the MYH7 gene.

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Nucleotide