PAH c.1043T>C ;(p.L348P)

Variant ID: 12-103238136-A-G

NM_000277.1(PAH):c.1043T>C;(p.L348P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Characterization of phenylalanine hydroxylase gene variants and analysis of genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China.

Molecular Biology Reports
Zhou, Jinfu J; Zeng, Yinglin Y; Qiu, Xiaolong X; Lin, Qingying Q; Chen, Weifeng W; Luo, Jinying J; Xu, Liangpu L
Publication Date: 2022-11

Variant appearance in text: PAH: Leu348Pro
PubMed Link: 36104584
Variant Present in the following documents:
  • Main text
  • 11033_2022_Article_7579.pdf
View BVdb publication page



The Predictive Value of Genetic Analyses in the Diagnosis of Tetrahydrobiopterin (BH4)-Responsiveness in Chinese Phenylalanine Hydroxylase Deficiency Patients.

Scientific Reports
Zhu, Tianwen T; Ye, Jun J; Han, Lianshu L; Qiu, Wenjuan W; Zhang, Huiwen H; Liang, Lili L; Gu, Xuefan X
Publication Date: 2017-07-28

Variant appearance in text: PAH: Leu348Pro
PubMed Link: 28754886
Variant Present in the following documents:
View BVdb publication page