Kaiyrzhanov, R; Zaki, MS; Maroofian, R; Dominik, N; Rad, A; Vona, B; Houlden, H
(2021)
A Novel Homozygous ADCY5 Variant is Associated with a Neurodevelopmental Disorder and Movement Abnormalities.
Mov Disord Clin Pract, 8 (7).
pp. 1140-1143.
ISSN 2330-1619
https://doi.org/10.1002/mdc3.13310
SGUL Authors: Maroofian, Reza
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Official URL: https://doi.org/10.1002/mdc3.13310
| Item Type: | Article | |||||||||||||||||||||||||||
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| Additional Information: | © 2021 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited. | |||||||||||||||||||||||||||
| Keywords: | ADCY5, autosomal recessive, dystonia, movement disorders, neurodevelopmental disorder, dystonia, autosomal recessive, ADCY5, neurodevelopmental disorder, movement disorders | |||||||||||||||||||||||||||
| SGUL Research Institute / Research Centre: | Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) | |||||||||||||||||||||||||||
| Journal or Publication Title: | Mov Disord Clin Pract | |||||||||||||||||||||||||||
| ISSN: | 2330-1619 | |||||||||||||||||||||||||||
| Language: | eng | |||||||||||||||||||||||||||
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| PubMed ID: | 34631954 | |||||||||||||||||||||||||||
| Web of Science ID: | WOS:000682562900001 | |||||||||||||||||||||||||||
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| URI: | https://openaccess.sgul.ac.uk/id/eprint/114572 | |||||||||||||||||||||||||||
| Publisher's version: | https://doi.org/10.1002/mdc3.13310 |
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