Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)

Cuvertino, S.; Hartill, V.; Colyer, A.; Garner, T.; Nair, N.; Al-Gazali, L.; Canham, N.; Faundes, V.; Flinter, F.; Hertecant, J.; Holder-Espinasse, M.; Jackson, B.; Lynch, S. A.; Nadat, F.; Narasimhan, V. M.; Peckham, M.; Sellers, R.; Seri, M.; Montanari, F.; Southgate, L.; Squeo, G. M.; Trembath, R.; Van Heel, D.; Venuto, S.; Weisberg, D.; Stals, K.; Ellard, S.; Barton, A.; Kimber, S. J.; Sheridan, E.; Merla, G.; Stevens, A.; Johnson, C. A.; Banka, S.

doi:10.1038/s41436-020-0784-7

Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.

Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3) / Cuvertino, S., Hartill, V., Colyer, A., Garner, T., Nair, N., Al-Gazali, L., Canham, N., Faundes, V., Flinter, F., Hertecant, J., Holder-Espinasse, M., Jackson, B., Lynch, S.A., Nadat, F., Narasimhan, V.M., Peckham, M., Sellers, R., Seri, M., Montanari, F., Southgate, L., et al.. - In: GENETICS IN MEDICINE. - ISSN 1098-3600. - 22:5(2020), pp. 980-980. [10.1038/s41436-020-0784-7]