MADHAVAN, Lashudaa Madura et al.
 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.
<strong>Medical Research Archives</strong>, [S.l.], v. 12, n. 11, nov. 2024.
ISSN 2375-1924.
Available at: &lt;<a href="https://esmed.org/MRA/mra/article/view/5942" target="_new">https://esmed.org/MRA/mra/article/view/5942</a>&gt;. Date accessed: 12 dec. 2024.
doi: <a href="https://doi.org/10.18103/mra.v12i11.5942">https://doi.org/10.18103/mra.v12i11.5942</a>.