Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variantJeroen J. Smits, M. F. van Dooren, Sarina G. Kant et al.|Human Genetics|2021Cited by 16
Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9Dorien Verdoodt, Erik de Vrieze|Hearing Research|2023Cited by 5
Exploring the Missing Heritability in Subjects With Hearing Loss, Enlarged Vestibular Aqueducts, and A Single or No Pathogenic SLC26A4 VariantJeroen J. Smits, Hannie Kremer, Suzanne E. de Bruijn et al.|Research Square|2021Cited by 2
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variantJeroen J. Smits, Suzanne E. de Bruijn, Cris Lanting et al.|Human Genetics|2021Cited by 0