Associated Papers
Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome.
Qin Z et al.
Frontiers in Genetics, 2020
32625235 (PubMed )
Supplement: Data_Sheet_1.zip › Supplementary_Table_2.XLSX › patient_5
Efficient Mining of Variants From Trios for Ventricular Septal Defect Association Study.
Jiang P et al.
Frontiers in Genetics, 2019
31440271 (PubMed )
Supplement: Table_1.xlsx › SS-based_coding_variants
[Effect of Arg188Gln (G/A) mutation on enzymatic activity of kynureninase].
Shen J et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences, 2017
A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population.
Zhang Y et al.
Circulation. Cardiovascular Genetics, 2011
[A polymorphism of kynureninase gene in a hypertensive candidate chromosomal region is associated with essential hypertension].
Zhang Y et al.
Zhonghua Xin Xue Guan Bing Za Zhi, 2005
Genetic alterations affecting the genes encoding the enzymes of the kynurenine pathway and their association with human diseases.
Boros FA et al.
Mutation Research. Reviews in Mutation Research, 0
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