A. Alexeeva

发表

The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology

A. Fisenko, I. Zhanin, A. Pakhomov, 2022, Orphanet Journal of Rare Diseases.

Genotype–Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants

A. Pushkov, I. Zhanin, A. Pakhomov, 2023, Genes.