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Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)—an update

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journal contribution
posted on 04.03.2021, 17:19 by A Aamir, HJ Kuht, K Grønskov, BP Brooks, MG Thomas
Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)—an update

Funding

EuroGentest2 (Unit 2: “Genetic testing as part of health care”), a Coordination Action under FP7 (Grant Agreement Number 261469) and the European Society of Human Genetics. We acknowledge the support of Fight for Sight, Academy of Medical Sciences, Ulverscroft Foundation, National Institute of Health Research and Medical Research Council. MGT is supported by the NIHR (CL-2017-11-003). MGT acknowledges the support of Fight for Sight, Ulverscroft Foundation, Medical Research Council, National Institute of Health Research (CL-2017-11-003) and Academy of Medical Sciences.

History

Citation

Eur J Hum Genet (2021). https://doi.org/10.1038/s41431-021-00809-w

Author affiliation

Department of Neuroscience, Psychology and Behaviour, College of Life Sciences

Version

AM (Accepted Manuscript)

Published in

European Journal of Human Genetics

Publisher

Springer Science and Business Media LLC

issn

1018-4813

eissn

1476-5438

Acceptance date

08/01/2021

Copyright date

2021

Available date

27/07/2021

Language

en