Centre de Référence Déficits Immunitaires Héréditaires
Parent institutions Hôpital Necker-Enfants Malades, Inserm
ROR: Yes
Works count: 1,105
Citations count: 38,920
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
1999 · Christian Kubisch, Björn C. Schroeder, et al. · Cell
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
2003 · Catherine Dodé, Jacqueline Levilliers, et al. · Nature Genetics