Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.
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The number of electrons in the outermost shell of an atom
Answer:
Am I supposed to tell you if it's right or wrong? or what...??
Explanation:
One possible result of chromosomal breakage is for a fragment to join a nonhomologous chromosome. What is this type of chromosomal alteration called <u>translocation.</u>
A chromosomal fragment is translocated when it is moved from one genomic sequence to another. Around two nonhomologous chromosomes, a translocation mechanism takes place in order to permit the interchange of fragments created by chromosomal breakage.
When a segment of one chromosome separates and affixes towards another chromosome, translocation takes place. If there is neither genetic material growth nor loss in the cell, such a form of rearrangement would be referred to as balanced.
To learn more about nonhomologous chromosome here
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