Additional file 1 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme

Lewis, Morag A.; Ingham, Neil J.; Chen, Jing; Pearson, Selina; Di Domenico, Francesca; Rekhi, Sohinder; Allen, Rochelle; Drake, Matthew; Willaert, Annelore; Rook, Victoria; Pass, Johanna; Keane, Thomas; Adams, David J.; Tucker, Abigail S.; White, Jacqueline K.; Steel, Karen P.

doi:10.6084/m9.figshare.19373358.v1

12915_2022_1257_MOESM1_ESM.pdf (6.47 MB)

Additional file 1 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme

journal contribution

posted on 2022-03-17, 04:31 authored by Morag A. Lewis, Neil J. Ingham, Jing Chen, Selina Pearson, Francesca Di Domenico, Sohinder Rekhi, Rochelle Allen, Matthew Drake, Annelore Willaert, Victoria Rook, Johanna Pass, Thomas Keane, David J. Adams, Abigail S. Tucker, Jacqueline K. White, Karen P. Steel

Additional file 1.

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wellcome trust medical research council european commission biotechnology and biological sciences research council research foundation flanders

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Spontaneous mutations Large-scale mutagenesis programme Deafness Progressive hearing loss Non-segregating phenotypes

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Additional file 1 of Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme

Funding

wellcome trust medical research council european commission biotechnology and biological sciences research council research foundation flanders

History

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