The discoverer of Canavan syndrome gene: how problems of diagnosis and treatment are being changed over time
| dc.contributor.author | Grechanina, Elena | |
| dc.contributor.author | Grechanina, Juliya | |
| dc.contributor.author | Matalon, Reuben | |
| dc.contributor.author | Delgado, Listvania | |
| dc.contributor.author | Tyring, Stephen | |
| dc.date.accessioned | 2019-11-22T07:23:04Z | |
| dc.date.available | 2019-11-22T07:23:04Z | |
| dc.date.issued | 2019-06-04 | |
| dc.description.abstract | Canavan disease is an autosomal recessive degenerative disorder that causes progressive damage to nerve cells in the brain, and is one of the most common degenerative cerebral diseases of infancy. | ru_RU |
| dc.identifier.citation | The discoverer of Canavan syndrome gene: how problems of diagnosis and treatment are being changed over time / E. Grechanina, Yu. Grechanina, R. Matalon, L. M. Delgado, S. K. Tyring // Клінічна генетика і перинатальна діагностика. – 2019. – № 1 (6). – С. 53–97. | ru_RU |
| dc.identifier.uri | https://repo.knmu.edu.ua/handle/123456789/24827 | |
| dc.language.iso | en | ru_RU |
| dc.publisher | Український інститут клінічної генетики ХНМУ | ru_RU |
| dc.subject | Canavan disease | ru_RU |
| dc.title | The discoverer of Canavan syndrome gene: how problems of diagnosis and treatment are being changed over time | ru_RU |
| dc.type | Article | ru_RU |