Search

Search Constraints

You searched for: Author/Creator Ashley, Euan A.

Search Results

2. A Premature Termination Codon Mutation in MYBPC3 Causes Hypertrophic Cardiomyopathy via Chronic Activation of Nonsense-Mediated Decay. Issue 6 (5th February 2019)

3. A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases. Issue 7 (11th September 2015)

4. A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Issue 2 (9th April 2019)

5. Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation. Issue 9 (27th August 2019)

7. Associations Between Female Sex, Sarcomere Variants, and Clinical Outcomes in Hypertrophic Cardiomyopathy. (February 2021)

8. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma. (August 2018)