Varaico: Literature-Extracted Genetic Variants

Gene:PAH
Variant:p.G239D
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PAH

NM_000277.3:p.G239D

Associated Papers

Diagnostic yield of expanded carrier screening of a multi-ethnic population in yunnan, China.

Wang H et al.

Scientific Reports, 2025

40604033 (PubMed )
Supplement: 41598_2025_8012_MOESM1_ESM.xlsx › S3

Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China.

Chen T et al.

Scientific Reports, 2018

Analysis of the genotype-phenotype correlation in patients with phenylketonuria in mainland China.

Li N et al.

Scientific Reports, 2018

Mutation spectrum of hyperphenylalaninemia candidate genes and the genotype-phenotype correlation in the Chinese population.

Wang R et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2018

[Research progress on phenotype and genotype of hyperphenylalaninemia].

Chen T et al.

Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences, 2018

Molecular characterisation of phenylketonuria in a Chinese mainland population using next-generation sequencing.

Li N et al.

Scientific Reports, 2015

Mutation spectrum of six genes in Chinese phenylketonuria patients obtained through next-generation sequencing.

Gu Y et al.

Plos One, 2014

Variations in genotype-phenotype correlations in phenylalanine hydroxylase deficiency in Chinese Han population.

Zhu T et al.

Gene, 2013

Mutational spectrum of phenylketonuria in the Chinese Han population: a novel insight into the geographic distribution of the common mutations.

Zhu T et al.

Pediatric Research, 2010

Phenylketonuria mutations in Northern China.

Song F et al.

Molecular Genetics and Metabolism, 2005

[Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria].

Zhang J et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2005

[Mutations in exon 7 of the phenylalanine hydroxylase (PAH) gene in chinese patients with phenylketonuria].

Song F et al.

Yi Chuan = Hereditas, 2005

[Ten novel mutations in the phenylalanine hydroxylase gene identified in Chinese patients with phenylketonuria].

Song F et al.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae, 2003

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."