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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awdur: Haskins, Mark E
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2007
Pynciau:
Mynediad Ar-lein: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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