De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Titel:
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Auteur:
Smits, Jeroen J. Oostrik, Jaap Beynon, Andy J. Kant, Sarina G. Koning Gans, Pia A. M. de Rotteveel, Liselotte J. C. Klein Wassink-Ruiter, Jolien S. Free, Rolien H. Maas, Saskia M. Kamp, Jiddeke van de Merkus, Paul Koole, Wouter Feenstra, Ilse Admiraal, Ronald J. C. Lanting, Cornelis P. Schraders, Margit Yntema, Helger G. Pennings, Ronald J. E. Kremer, Hannie