King-Robson, J; Marshall, J; Smith, F; Willoughby, L; Mansour, S; Sztriha, L
(2021)
Ataxia-Pancytopenia Syndrome due to a de Novo SAMD9L Mutation.
Neurol Genet, 7 (3).
e580.
ISSN 2376-7839
https://doi.org/10.1212/NXG.0000000000000580
SGUL Authors: Mansour, Sahar
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Official URL: https://doi.org/10.1212/NXG.0000000000000580
| Item Type: | Article | ||||||||
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| Additional Information: | Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. | ||||||||
| SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) | ||||||||
| Journal or Publication Title: | Neurol Genet | ||||||||
| ISSN: | 2376-7839 | ||||||||
| Language: | eng | ||||||||
| Dates: |
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| Publisher License: | Creative Commons: Attribution 4.0 | ||||||||
| PubMed ID: | 33884299 | ||||||||
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| URI: | https://openaccess.sgul.ac.uk/id/eprint/113641 | ||||||||
| Publisher's version: | https://doi.org/10.1212/NXG.0000000000000580 |
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