Biology, 17.11.2020 18:50 cristinavalencia03
Tay-Sachs disease is a rare, inherited disorder that most commonly affects
infants. There are typically no symptoms evident in the first 3-6 months of life.
After the first 3-6 months, development slows, motor skills diminish and
ultimately premature death results. The cause of this disease is the inability to
produce enough functional hexosaminidase A (Hex-A). Hex-A is an enzyme
that cleaves (cuts up) certain waste lipids in the brain and spinal cord.
Based on these details, where in the cell does Hex-A most likely reside?
O points
Cytoplasm
Ο Ο
Nucleus
Lysosome
Mitochondria
Answers: 1
Biology, 21.06.2019 16:30
Wht happens as electrons in the electron transport chain release their energy
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Biology, 21.06.2019 23:50
Differentiation of cells changes the nucleic information. true false
Answers: 2
Tay-Sachs disease is a rare, inherited disorder that most commonly affects
infants. There are typic...
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