A novel Pah-exon1 deleted murine model of phenylalanine hydroxylase (PAH) deficiency.
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| Title: | A novel Pah-exon1 deleted murine model of phenylalanine hydroxylase (PAH) deficiency. |
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| Authors: | Richards DY; Department of Medical and Molecular Genetics, Oregon Health & Science University, Portland, USA., Winn SR; Department of Medical and Molecular Genetics, Oregon Health & Science University, Portland, USA., Dudley S; Department of Medical and Molecular Genetics, Oregon Health & Science University, Portland, USA., Fedorov L; Transgenic Mouse Models Core, Oregon Health and Science University, Portland, USA., Rimann N; Division of Metabolism, University Children's Hospital, Steinweissstrasse 75, Zurich CH-8032, Switzerland., Thöny B; Division of Metabolism, University Children's Hospital, Steinweissstrasse 75, Zurich CH-8032, Switzerland., Harding CO; Department of Medical and Molecular Genetics, Oregon Health & Science University, Portland, USA. Electronic address: hardingc@ohsu.edu. |
| Source: | Molecular genetics and metabolism [Mol Genet Metab] 2020 Nov; Vol. 131 (3), pp. 306-315. Date of Electronic Publication: 2020 Sep 30. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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