(2024) ELFN1 deficiency is associated with an autosomal recessive neurodevelopmental disorder with epilepsy. European Journal of Human Genetics. pp. 1510-1511. ISSN 1018-4813
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| Item Type: | Article |
|---|---|
| Keywords: | Biochemistry & Molecular Biology Genetics & Heredity |
| Page Range: | pp. 1510-1511 |
| Journal or Publication Title: | European Journal of Human Genetics |
| Journal Index: | ISI |
| Volume: | 32 |
| ISSN: | 1018-4813 |
| Depositing User: | خانم ناهید ضیائی |
| URI: | http://eprints.mui.ac.ir/id/eprint/30056 |
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