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Impaired fertility and motor function in a zebrafish model for classic galactosemia
Classic galactosemia is a genetic disorder of galactose metabolism, caused by severe deficiency of galactose-1-phosphate uridylyltransferase (GALT) enzyme activity due to mutations of the GALT gene. Its pathogenesis is still not fully elucidated, and a therapy that prevents chronic impairments is la...
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| 發表在: | J Inherit Metab Dis |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer Netherlands
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5786655/ https://ncbi.nlm.nih.gov/pubmed/28913702 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-017-0071-1 |
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