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Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type
Combined methylmalonic acidemia and homocystinuria, cblC type, is the most common inherited disorder of cobalamin metabolism and is characterized by severe fetal developmental defects primarily impacting the central nervous system, hematopoietic system, and heart. CblC was previously shown to be due...
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| Publicat a: | Dev Biol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7669717/ https://ncbi.nlm.nih.gov/pubmed/32941884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2020.09.005 |
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