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Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1.
Aponte, J L; Sega, G A; Hauser, L J; Dhar, M S; Withrow, C M; Carpenter, D A; Rinchik, E M; Culiat, C T; Johnson, D K.
Affiliation
  • Aponte JL; Division of Biology, University of Tennessee, Knoxville, TN 37996-0910, USA.
Proc Natl Acad Sci U S A ; 98(2): 641-5, 2001 Jan 16.
Article in En | MEDLINE | ID: mdl-11209059

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Tyrosinemias / Genes / Hydrolases Language: En Journal: Proc Natl Acad Sci U S A Year: 2001 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Tyrosinemias / Genes / Hydrolases Language: En Journal: Proc Natl Acad Sci U S A Year: 2001 Document type: Article Affiliation country: Country of publication: