Functional muscle analysis of the Tcap knockout mouse
Chad D. Markert(Forest Institute), Martin K. Childers(University of Washington), Stephen J. Walker(Forest Institute), Robert W. Grange(Virginia Tech), Michael W. Lawlor(Medical College of Wisconsin), Mary Pat Meaney(Appalachian State University), H. W. Dalley(Virginia Tech), Alan H. Beggs(Boston Children's Hospital), S. X. Yu(Ingenious Targeting Laboratory (United States)), Maryam Ahmed(Forest Institute), M. Brown(University of Missouri), Kevin A. Voelker(Virginia Tech), B. Bishwokarma(Forest Institute), Jennifer K. Cann(Forest Institute)
Cited by 54
Related Papers
Genotype-Phenotype Correlation in the Long-QT Syndrome
|Circulation|2001|1.8k
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
|Nature Genetics|2000|1.3k
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
|PubMed|1989|961
ACTN3 Genotype Is Associated with Human Elite Athletic Performance
|The American Journal of Human Genetics|2003|917
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing
|Science Translational Medicine|2017|809