Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction

Wesdorp, M.; Gans, P.A.M.D.; Schraders, M.; Oostrik, J.; Huynen, M.A.; Venselaar, H.; ... ; DOOFNL Consortium (2018)

Article / Letter to editor

• All authors: Wesdorp, M.; Gans, P.A.M.D.; Schraders, M.; Oostrik, J.; Huynen, M.A.; Venselaar, H.; Beynon, A.J.; Gaalen, J. van; Piai, V.; Voermans, N.; Rossum, M.M. van; Hartel, B.P.; Lelieveld, S.H.; Wiel, L.; Verbist, B.; Rotteveel, L.J.; Dooren, M.F. van; Lichtner, P.; Kunst, H.P.M.; Feenstra, I.; Admiraal, R.J.C.; Yntema, H.G.; Hoefsloot, L.H.; Pennings, R.J.E.; Kremer, H.; DOOFNL Consortium
• Date: 2018-05-31
• Journal: Human Genetics
• Volume: 137
• Issue: 5
• Pages: 389 - 400
• DOI: doi:10.1007/s00439-018-1880-5
• Link: https://link.springer.com/content/pdf/10.1007/s00439-018-1880-5.pdf