Literature DB >> 2516180

Twenty-one cases of phenylketonuria out of 358,767 newborns in Shanghai, China.

R G Chen1, X S Pan, D L Qian, H Guo.   

Abstract

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Year:  1989        PMID： 2516180     DOI： 10.1007/bf01802047

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

1.  Phenylketonuria mutations in southern Chinese detected by denaturing gradient gel electrophoresis in exon 7 of PAH gene.

Authors:  X F Gu; M Zhang; R G Chen
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

2.  Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Andrea V Margulis; Kimberly Alexander; Renee Shediac; Brian Calingaert; Abenah Harding; Manel Pladevall-Vila; Sarah Landis
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

3.  Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

Authors:  Hamid Reza Shoraka; Ali Akbar Haghdoost; Mohammad Reza Baneshi; Zohre Bagherinezhad; Farzaneh Zolala
Journal:  Clin Exp Pediatr       Date:  2020-02-06
  3 in total

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