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You searched for: Author/Creator Ehler, Elisabeth

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4. CMYA5 is a novel interaction partner of FHL2 in cardiac myocytes. (27th February 2022)

5. Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. (October 2016)

6. Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion. (August 2018)

10. Small change, big impact: A Z-disc missense genetic variant causes dramatic morphological changes in the embryonic heart. (31st December 2022)