#Question id: 4110
#Unit 3. Fundamental Processes
Tay-Sachs disease belongs to the family of lysosomal storage diseases; it is an autosomal recessive neurodegenerative disorder caused by deficiency of the lysosomal enzyme hexosaminidase. The inability to degrade sphingolipids results in the deposition of these lipids in the cells that causes severe mental retardation and death in childhood. The most common mutation in Tay-Sachs disease patients is a 4-base pair insertion in exon 11 of the 14 exons of the hexosaminidase gene. What could be the most likely consequence of this mutation?
#Question id: 12780
#Unit 10. Ecological Principles
#Question id: 8922
#Unit 9. Diversity of Life Forms
#Question id: 6968
#Unit 5. Developmental Biology
In Xenopus, the mesoderm moves in through the blastopore by rolling around the dorsal lip in a process called:
#Question id: 12649
#Unit 6. System Physiology – Plant