Please use this identifier to cite or link to this item:
http://repo.knmu.edu.ua/handle/123456789/24827Full metadata record
| DC Field | Value | Language |
|---|---|---|
| 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.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.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.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 |
| Appears in Collections: | Наукові праці. Кафедра медичної генетики | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| The discoverer of Canavan syndrome gene.pdf | 12,08 MB | Adobe PDF |  View/Open |
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