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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

Jeroen J. Smits; Jaap Oostrik; Andy J. Beynon; Sarina G. Kant; Pia A. M. de Koning Gans; Liselotte J. C. Rotteveel; Jolien S. Klein Wassink-Ruiter; Rolien H. Free; Saskia M. Maas; Jiddeke van de Kamp; Paul Merkus; Wouter Koole; Ilse Feenstra; Ronald J. C. Admiraal; Cornelis P. Lanting; Margit Schraders; Helger G. Yntema; Ronald J. E. Pennings; Hannie Kremer
Human Genetics · Vol. 138, Issue 1 · pp. 61-72 · 2019
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2019-01-01
Publication Year2019
Volume138
Issue1
Pages61-72
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-018-1965-1

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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