Associated Papers
HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810K.
Xu J et al.
European Journal of Neurology, 2024
39315749 (PubMed )
Supplement: ENE-31-e16473-s001.xlsx › Table_S2
Disruption of PIKFYVE causes congenital cataract in human and zebrafish.
Mei S et al.
Elife, 2022
The Role of Formyl Peptide Receptor 1 Gene Polymorphisms in Human Colorectal Cancer.
Li SQ et al.
Journal of Cancer, 2020
Formyl Peptide Receptor Polymorphisms: 27 Most Possible Ways for Phagocyte Dysfunction.
Skvortsov SS et al.
Biochemistry. Biokhimiia, 2017
FPR1 interacts with CFH, HTRA1 and smoking in exudative age-related macular degeneration and polypoidal choroidal vasculopathy.
Liang XY et al.
Eye (london, England), 2014
Neutrophil formylpeptide receptor single nucleotide polymorphism 348T>C in aggressive periodontitis.
Maney P et al.
Journal of Periodontology, 2009
[Restrictive fragment length polymorphism analysis of gamma-crystallin in congenital cataract families].
Lu S et al.
Yan Ke Xue Bao = Eye Science, 1994
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