Please use this identifier to cite or link to this item:
https://doi.org/10.1111/cge.12031
| Title: | Mutations in ATP1A3 cause alternating hemiplegia of childhood | Authors: | Aminkeng, F | Keywords: | Science & Technology Life Sciences & Biomedicine Genetics & Heredity ONSET |
Issue Date: | 1-Jan-2013 | Publisher: | WILEY | Citation: | Aminkeng, F (2013-01-01). Mutations in ATP1A3 cause alternating hemiplegia of childhood. CLINICAL GENETICS 83 (1) : 32-33. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12031 | Abstract: | Heterozygous de novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. Rosewich et al. (2012) Lancet Neurology 11(9):764-773. © 2012 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd. | Source Title: | CLINICAL GENETICS | URI: | https://scholarbank.nus.edu.sg/handle/10635/235311 | ISSN: | 0009-9163 1399-0004 |
DOI: | 10.1111/cge.12031 |
| Appears in Collections: | Staff Publications Elements |
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