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Diagnosis, treatment and outcome of glutaric aciduria type I in Zhejiang Province, China
BACKGROUND: Glutaric aciduria type I (GA I; MIM 231670) is a rare autosomal recessive disorder resulting from glutaryl-CoA dehydrogenase deficiency. This article reports our experience in the diagnosis, treatment and outcome of GA I patients in Zhejiang Province, China. MATERIAL/METHODS: A total of...
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| Главные авторы: | , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
International Scientific Literature, Inc.
2011
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3539576/ https://ncbi.nlm.nih.gov/pubmed/21709643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.881834 |
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