Rajagopalan, Ramakrishnan

Protein‐elongating mutations inMYH11are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

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

Human Mutation | January 16, 2020 | Volume: 41 | Issue: 5 | Pages: 973-982

10.1002/humu.23986