Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome
Bethan E. Hoskins(University of Michigan), Friedhelm Hildebrandt(Boston Children's Hospital), Derek Silvius(Boys Town), Dan Zou(McLaughlin Research Institute), Dana J. Orten(Boys Town National Research Hospital), Edgar A. Otto(University of Michigan), Pin‐Xian Xu(Brigham and Women's Hospital), Dominique Weil(Boys Town), Christine Petit(Centre National de la Recherche Scientifique), Carl H. Cramer(Mayo Clinic), Richard M. Raymond(Boys Town), William J. Kimberling(Boys Town), Richard J. Smith(University of Iowa)
Cited by 203
Related Papers
A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration
|Proceedings of the National Academy of Sciences|2005|2k
Ciliopathies
|New England Journal of Medicine|2011|1.4k
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
|Cell|1999|868
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
|Nature Genetics|1999|718
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
|Journal of the American Society of Nephrology|2014|660