Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases

Hedwig M. Velde, Maryam Vaseghi-Shanjani, DOOFNL Consortium, Jeroen J. Smits, Gayatri Ramakrishnan, Jaap Oostrik, Mieke Wesdorp, Galuh Astuti, H. G. Yntema, E. H. Hoefsloot, Cris P. Lanting, Martijn A. Huynen, Anna Lehman, Stuart E. Turvey, Ronald J.E. Pennings, Hannie Kremer*

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Biochemistry, Genetics and Molecular Biology