Selenoprotein N deficiency in mice is associated with abnormal lung development
Behzad Moghadaszadeh(Boston Children's Hospital), Alan H. Beggs(Boston Children's Hospital), Caroline A. Owen(Brigham and Women's Hospital), Robert W. Grange(Virginia Tech), Michael W. Lawlor(Medical College of Wisconsin), Steve Boukedes(Brigham and Women's Hospital), Branden E. Rider(Boston Children's Hospital), Kushagra Gupta(Pulmonary and Critical Care Associates), Martin K. Childers(University of Washington)
Cited by 41
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