Protein-elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Melissa A. Gilbert, Laura Schultz-Rogers, Ramakrishnan Rajagopalan, Christopher M. Grochowski, Benjamin J. Wilkins, Sawona Biswas, Laura K. Conlin, Kristin N. Fiorino, Radhika Dhamija, Michael A. Pack, Eric W. Klee, David A. Piccoli, Nancy B. Spinner

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Fingerprint

Dive into the research topics of 'Protein-elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease'. Together they form a unique fingerprint.

Medicine & Life Sciences