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A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.
- Published in:
- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101750
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- Publication type:
- Article
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.
- Published in:
- Genes, 2022, v. 13, n. 2, p. 309, doi. 10.3390/genes13020309
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- Publication type:
- Article
The LDLR , APOB , and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
- Published in:
- Genes, 2021, v. 12, n. 1, p. 66, doi. 10.3390/genes12010066
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- Publication type:
- Article
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7556, doi. 10.3390/ijms25147556
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- Article