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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
Velde, H. M., Vaseghi-Shanjani, M., Smits, J. J., Ramakrishnan, G., Oostrik, J., Wesdorp, M., Astuti, G., Yntema, H. G., Hoefsloot, L., Lanting, C. P., Huynen, M. A., Lehman, A., Turvey, S. E. & DOOFNL Consortium, Nov 2024, In: Human genetics. 143, 11, p. 1379-1399 21 p.Research output: Contribution to journal › Article* › Academic › peer-review
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