In Vitro Expression of 34 Naturally Occurring Mutant Variants of Phenylalanine Hydroxylase: Correlation with Metabolic Phenotypes and Susceptibility toward Protein Aggregation-Reference-Cited by-同舟云学术

In Vitro Expression of 34 Naturally Occurring Mutant Variants of Phenylalanine Hydroxylase: Correlation with Metabolic Phenotypes and Susceptibility toward Protein Aggregation

Published:2001-02 Issue:2 Volume:72 Page:132-143
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Gjetting Torben,Petersen Marie,Guldberg Per,Güttler Flemming

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference45 articles.

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2. Hyperphenylalaninemia: Diagnosis and classification of the various types of phenylalanine hydroxylase deficiency;Güttler;Acta Paediatr Scand,1980

3. PAHdb: www.mcgill.ca/pahdb.

4. PAHdb: A locus-specific knowledgebase;Scriver;Hum Mutat,2000

5. Prediction of multiple hypermutable codons in the human PAH gene: Codon 280 contains recurrent mutations in Quebec and other populations;Byck;Hum Mutat,1997

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