Exploring Liposyn II’s Potential Impact on Sandhoff Disease Treatmen
Understanding Sandhoff Disease: Genetic Foundations and Challenges Understanding Sandhoff disease begins with its genetic roots, as it is a rare and inherited disorder resulting from the mutation of the HEXB gene. This mutation leads to the deficiency of the Hexosaminidase B enzyme, crucial for breaking down specific lipids in the body. The absence of this […]
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