Perturbation of the titin/MURF1 signaling complex is associated with hypertrophic cardiomyopathy in a fish model and in human patients
Hypertrophic cardiomyopathy (HCM) is a hereditary disease characterized by cardiac hypertrophy with diastolic dysfunction. Gene mutations causing HCM have been found in about half of HCM patients, while the genetic etiology and pathogenesis remain unknown for many cases of HCM. To identify novel mec...
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Materyal Türü: | Kitap |
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The Company of Biologists,
2019-11-01T00:00:00Z.
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A1234.567 |
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Kopya Bilgisi 1 | Kütüphanede |