Transcriptional profile of postmortem skeletal muscle
Despina Sanoudou(National and Kapodistrian University of Athens), Alan H. Beggs(Boston Children's Hospital), Louis M. Kunkel(Boston Children's Hospital), Peter B. Kang(Boston Children's Hospital), Mei Han(First Affiliated Hospital of Xiamen University), Judith N. Haslett(Brigham and Women's Hospital)
Cited by 51
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