Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome
Martin Vollmer(University Medical Center Freiburg), Friedhelm Hildebrandt(Boston Children's Hospital), Heymut Omran(University Hospital Münster), Brigitte Strahm(University Medical Center Freiburg), Rezan Topaloğlu(Hacettepe University), Martin Koehrer(University Medical Center Freiburg)
Cited by 46
Related Papers
Ciliopathies
|New England Journal of Medicine|2011|1.4k
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
|Journal of the American Society of Nephrology|2014|660
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
|Nature Genetics|2011|658