Whole genome sequencing reveals a 7 base-pair deletion in DMD exon 42 in a dog with muscular dystrophy
Peter P. Nghiem(Texas A&M University), Joe N. Kornegay(Texas A&M University), Briana Hernandez(Texas A&M University), Luca Bello(Children's National), Amanda K. Bettis(Texas A&M University), Scott J. Schatzberg(Georgia College & State University), Sara Mata López(Texas A&M University), Heather H. Barnett(Texas A&M University), Richard J. Piercy(Royal Veterinary College), Cindy Balog‐Alvarez
Cited by 26
Related Papers
Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies
|Mammalian Genome|2012|178
Functional changes in Duchenne muscular dystrophy
|Neurology|2011|178
Transient MPK6 activation in response to oxygen deprivation and reoxygenation is mediated by mitochondria and aids seedling survival in Arabidopsis
|Plant Molecular Biology|2011|146
Magnetic Resonance Imaging in Dogs with Neurologic Impairment Due to Acute Thoracic and Lumbar Intervertebral Disk Herniation
|Journal of Veterinary Internal Medicine|2009|118
The Paradox of Muscle Hypertrophy in Muscular Dystrophy
|Physical Medicine and Rehabilitation Clinics of North America|2012|111