Long-term preservation of intellectual functioning in sapropterin-treated infants and young children with phenylketonuria: A seven-year analysis-Reference-Cited by-同舟云学术

Long-term preservation of intellectual functioning in sapropterin-treated infants and young children with phenylketonuria: A seven-year analysis

Published:2021-02 Issue:2 Volume:132 Page:119-127
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Waisbren Susan,Burton Barbara K.,Feigenbaum Annette,Konczal Laura L.,Lilienstein Joshua,McCandless Shawn E.,Rowell Richard,Sanchez-Valle Amarilis,Whitehall Kaleigh B.,Longo Nicola

Funder

BioMarin Pharmaceutical

Publisher

Elsevier BV

Subject

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

Reference40 articles.

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4. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014

5. The complete European guidelines on phenylketonuria: diagnosis and treatment;van Wegberg;Orphanet J. Rare Dis.,2017

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