National Institutes of Health (NIH) review of evidence in phenylalanine hydroxylase deficiency (phenylketonuria) and recommendations/guidelines for therapy from the American College of Medical Genetics (ACMG) and Genetics Metabolic Dietitians International (GMDI)
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference7 articles.
1. Phenylketonuria scientific review conference: state of the science and future research needs;Camp;Mol. Genet. Metab.,2014
2. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014
3. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency;Singh;Genet. Med.,2014
4. Early-treated phenylketonuria: adult neuropsychologic outcome;Ris;J. Pediatr.,1994
5. Executive function in early-treated phenylketonuria: profile and underlying mechanisms;Christ;Mol. Genet. Metab.,2010
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