Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene-Reference-Cited by-同舟云学术

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Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene

Published:1988-04-19 Issue:8 Volume:27 Page:2881-2885
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Lichter-Konecki Uta,Konecki David S.,DiLella Anthony G.,Brayton Kelly,Marvit Joshua,Hahn Tina M.,Trefz Fritz K.,Woo Savio L. C.

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi00408a032

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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3. Relationship between genotype, phenylalanine hydroxylase expression and in vitro activity and metabolic phenotype in phenylketonuria;Molecular Genetics and Metabolism;2018-09

4. The Yeast Ubr1 Ubiquitin Ligase Participates in a Prominent Pathway That Targets Cytosolic Thermosensitive Mutants for Degradation;G3 Genes|Genomes|Genetics;2012-05-01

5. Structural and mechanistic implications of incorporating naturally occurring aberrant mutations of human dihydropteridine reductase into a rat model;International Journal of Peptide and Protein Research;2009-01-12

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