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Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1

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Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Main Authors: Aponte, Jennifer L., Sega, Gary A., Hauser, Loren J., Dhar, Madhu S., Withrow, Catherine M., Carpenter, Donald A., Rinchik, Eugene M., Culiat, Cymbeline T., Johnson, Dabney K.
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 2001
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC14641/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11209059/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.98.2.641
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