Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant
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Published:2021-10-04
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ISSN:0340-6717
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Container-title:Human Genetics
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language:en
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Short-container-title:Hum Genet
Author:
Smits Jeroen J.ORCID, de Bruijn Suzanne E.ORCID, Lanting Cornelis P.ORCID, Oostrik Jaap, O’Gorman Luke, Mantere Tuomo, van Dooren M. F., Kant S. G., de Gier H. H. W., Hoefsloot E. H., van der Schroeff M. P., Rotteveel L. J. C., Ropers F. G., Widdershoven J. C. C., Hof J. R., Vanhoutte E. K., Feenstra I., Kremer H., Lanting C. P., Pennings R. J. E., Yntema H. G., Free R. H., Klein Wassink-Ruiter J. S., Stokroos R. J., Smit A. L., van den Boogaard M. J., Ebbens F. A., Maas S. M., Plomp A., Goderie T. P. M., Merkus P., van de Kamp J., Cremers Frans P. M.ORCID, Roosing Susanne, Yntema Helger G., de Vrieze Erik, Derks Ronny, Hoischen Alexander, Pegge Sjoert A. H., Neveling Kornelia, Pennings Ronald J. E.ORCID, Kremer HannieORCID,
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
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