Novel Causative Variants in DYRK1A, KARS, and KAT6A Associated with Intellectual Disability and Additional Phenotypic Features

Por Murray, Clark R., Abel, Samantha N., McClure, Matthew B., Foster, Joseph, Walke, Maria I., Jayakar, Parul, Bademci, Guney, Tekin, Mustafa
Publicado no J Pediatr Genet (2017)

Altered Cortical GABA(A) Receptor Composition, Physiology, and Endocytosis in a Mouse Model of a Human Genetic Absence Epilepsy Syndrome

Por Zhou, Chengwen, Huang, Zhiling, Ding, Li, Deel, M. Elizabeth, Arain, Fazal M., Murray, Clark R., Patel, Ronak S., Flanagan, Christopher D., Gallagher, Martin J.
Publicado em 2013

NAFLD Phosphoproteomics: A Functional Piece of the Precision Puzzle

Por Wattacheril, Julia, Rose, Kristie L., Hill, Salisha, Lanciault, Christian, Murray, Clark R., Washington, Kay, Williams, Brandon, English, Wayne, Spann, Matthew, Clements, Ronald, Abumrad, Naji, Flynn, Charles Robb
Publicado no Hepatol Res (2017)