PAH c.1085C>T ;(p.P362L)

Variant ID: 12-103237538-G-A

NM_000277.1(PAH):c.1085C>T;(p.P362L)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A capillary electrophoresis-based multiplex PCR assay for expanded carrier screening in the eastern Han Chinese population.

Npj Genomic Medicine
Hu, Ping P; Tan, Jianxin J; Yu, Feng F; Shao, Binbin B; Zhang, Fang F; Zhang, Jingjing J; Lin, Yingchun Y; Tao, Tao T; Jiang, Lili L; Jiang, Zhengwen Z; Xu, Zhengfeng Z
Publication Date: 2022-01-25

Variant appearance in text: PAH: 1085C>T
PubMed Link: 35079019
Variant Present in the following documents:
  • 41525_2021_280_MOESM1_ESM.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: Pro362Leu
PubMed Link: 28754886
Variant Present in the following documents:
View BVdb publication page



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

Scientific Reports
Li, Nana N; Jia, Haitao H; Liu, Zhen Z; Tao, Jing J; Chen, Song S; Li, Xiaohong X; Deng, Ying Y; Jin, Xi X; Song, Jiaping J; Zhang, Liangtao L; Liang, Yu Y; Wang, Wei W; Zhu, Jun J
Publication Date: 2015-10-27

Variant appearance in text: PAH: P362L
PubMed Link: 26503515
Variant Present in the following documents:
  • Main text
  • srep15769.pdf
View BVdb publication page