MC_UU_00007/4 Mouse Models of Human Variation and Disease

Jackson, Ian (Principal Investigator)

MRC Human Genetics Unit

Status	Finished
Effective start/end date	1/04/18 → 31/03/23

10 Article

The Dct−/− Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism
Tingaud-sequeira, A., Mercier, E., Michaud, V., Pinson, B., Gazova, I., Gontier, E., Decoeur, F., Mckie, L., Jackson, I. J., Arveiler, B. & Javerzat, S., 27 Jun 2022, In: Genes. 13, 7, p. 1164 1164.
Research output: Contribution to journal › Article › peer-review

Open Access
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A Mouse Model of Brittle Cornea Syndrome caused by mutation in Zfp469
Stanton, C., Findlay, A., Drake, C., Mustafa, Z., Gautier, P., McKie, L., Jackson, I. J. & Vitart, V., 22 Sept 2021, In: Disease Models and Mechanisms. 14, 9, dmm049175.
Research output: Contribution to journal › Article › peer-review

Open Access
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Dopachrome tautomerase variants in patients with oculocutaneous albinism
Pennamen, P., Tingaud-Sequeira, A., Gazova, I., Keighren, M., McKie, L., Marlin, S., Halem, S. G., Kaplan, J., Delevoye, C., Lacombe, D., Plaisant, C., Michaud, V., Lasseaux, E., Javerzat, S., Jackson, I. J. & Arveiler, B., 1 Mar 2021, In: Genetics in Medicine.
Research output: Contribution to journal › Article › peer-review

Open Access
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