Associated Papers
Rare variant analysis of PLXNA1 in Parkinson's disease in the Chinese population.
Li C et al.
Genes & Diseases, 2023
37397528 (PubMed )
Supplement: mmc1.pdf
Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.
Men M et al.
Molecular Genetics & Genomic Medicine, 2021
Select a paper to view details