Associated Papers
Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis.
Shinwari K et al.
Frontiers in Molecular Biosciences, 2022
Differences in molecular phenotype in mouse and human hypertrophic cardiomyopathy.
Vakrou S et al.
Scientific Reports, 2021
34162896 (PubMed )
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