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Animal models for mucopolysaccharidosis disorders and their clinical relevance
Progress in understanding how a particular genotype produces the phenotype of an inborn error of metabolism, such as a mucopolysaccharidosis, in human patients has been facilitated by the study of animals with mutations in the orthologous genes. These are not just animal models, but true orthologues...
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2007
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3351033/ https://ncbi.nlm.nih.gov/pubmed/17391445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1651-2227.2007.00211.x |
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