FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease
Caroline Ovaert; Tiffany Busa; Emilie Faure; Chantal Missirian; Nicole Philip; Florent Paoli; Mathieu Milh; Loic Macé; Stephane Zaffran
Author Information: Department of Pediatric and Congenital Cardiology, Timone Enfant
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