Search

Search Constraints

You searched for: Author/Creator Wright, Nathan T.

Search Results

2. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Issue 8 (5th May 2019)

3. Inherited Variants in SCARB1 Cause Severe Early-Onset Coronary Artery Disease. Issue 2 (12th May 2021)

5. Novel mutations in MYBPC1 are associated with myogenic tremor and mild myopathy. Issue 1 (17th May 2019)

6. Novel obscurins mediate cardiomyocyte adhesion and size via the PI3K/AKT/mTOR signaling pathway. (October 2017)