Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/10423| Title: | De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. | Authors: | Epi4K Consortium | Issue Date: | 28-Jul-2016 | Journal: | American journal of human genetics |
| Appears in Sites: | Publication workflow Queensland Health Publications |
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