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Tay-Sachs disease is a human genetic abnormality that results in cells accumulating and becoming clogged with very large and complex lipids Which cellular organelle must be involved in this condition?

Updated: 8/11/2023

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lysosomes

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Q: Tay-Sachs disease is a human genetic abnormality that results in cells accumulating and becoming clogged with very large and complex lipids Which cellular organelle must be involved in this condition?

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Related questions

Does TaySachs disease have a dominant or a recessive trait?

recessive

Does taysachs obey Mendel's law?

Tay-Sachs disease is a genetic disorder caused by a recessive mutation in the HEXA gene. It is an autosomal recessive disorder, meaning that it follows Mendel's law of inheritance. Two copies of the mutated gene are required for the disease to manifest.

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Tay-Sachs disease is a human genetic abnormality that results in cells accumulating and becoming clogged with very large and complex lipids Which cellular organelle must be involved in this condition?

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