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Spinner, Nancy B

0000-0001-8109-3648

Mayo Clinic

Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia and The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Citations 1

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 Get It