A novel Pah-exon1 deleted murine model of phenylalanine hydroxylase (PAH) deficiency.

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Bibliographic Details
Title: A novel Pah-exon1 deleted murine model of phenylalanine hydroxylase (PAH) deficiency.
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
Description
ISSN:1096-7206
DOI:10.1016/j.ymgme.2020.09.005