Author

Andrew T. Gunter

Institution: University of Mississippi Medical Center

Observed institution: University of Mississippi Medical Center

OpenAlex ID: A5059080036

Heterozygous variants inACTL6A, encoding a component of the BAF complex, are associated with intellectual disability

2017 · Ronit Marom, Mahim Jain, et al. · Human Mutation · 33

Diagnosis and management of the phenotypic spectrum of twins with Beckwith‐Wiedemann syndrome

2019 · Jennifer L. Cohen, Kelly A. Duffy, et al. · American Journal of Medical Genetics Part A · 24

Works count: 2

Citation count: 57

H-index: 2

I10-index: 2