Madhavan, L., 		Nagarajan, H., 		Vetrivel, U., & 		Jagadeesan, M.
2024 Nov 29.  In Silico Characterization of Two Adjacent Novel Homozygous Nucleotide Variations in the PEX6 Gene Predict L898V Mutation to Enhance Infantile Refsum Disease and Heimler Syndrome. Medical Research Archives. [Online] 12:11