Work

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

Year: 2020

Type: article

Source: Human Mutation

DOI: 10.1002/humu.23986

Authors: 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

Institutions: Children's Hospital of Philadelphia, University of Pennsylvania, Mayo Clinic, Mayo Clinic in Arizona

Language: English

Topic: Gastrointestinal motility and disorders

Subfield: Gastroenterology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2999702475

FWCI: 3.474

Cites: 39

Cited by: 29

Related to: 10