McNeill, A., Aurora, P., Rajput, K. et al. (4 more authors) (2022) Dominant and recessive SLC12A2-syndrome. American Journal of Medical Genetics Part A, 188 (3). pp. 996-999. ISSN 1552-4825
Metadata
| Item Type: | Article |
|---|---|
| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | © 2021 Wiley Periodicals LLC. This is an author-produced version of a paper subsequently published in The American Journal of Medical Genetics - Part A. Uploaded in accordance with the publisher's self-archiving policy. |
| Dates: |
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| Institution: | The University of Sheffield |
| Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Neuroscience (Sheffield) |
| Funding Information: | Funder Grant number Baily-Thomas Charitable Foundation TRUST/VC/AC/SG/5399-8436 National Institute for Health Research N/A |
| Depositing User: | Symplectic Sheffield |
| Date Deposited: | 22 Nov 2021 08:29 |
| Last Modified: | 19 Nov 2022 01:13 |
| Status: | Published |
| Publisher: | Wiley |
| Refereed: | Yes |
| Identification Number: | 10.1002/ajmg.a.62573 |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:180681 |
CORE (COnnecting REpositories)
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