GLYCOSYLATION DISORDER SYNDROME TYPE 1b: DIAGNOSTICS AND TREATMENT
The article highlights the medical case of a rare hereditary disease — glycosylation disorder syndrome type 1b, unique for our country. This syndrome is referred to the heterogeneous group of the congenital diseases characterized by the disorder of glycoprotein synthesis as a result of the defects N...
Tallennettuna:
| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Russo |
| Julkaistu: |
Union of pediatricians of Russia
2008-09-01
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| Sarja: | Педиатрическая фармакология |
| Linkit: | https://www.pedpharma.ru/jour/article/view/765 |
| Tagit: |
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