This is happen during anaphase when two chromatids separate and move towards opposite poles,
Answer:
(A). Result in different amino acids to be read due to frame shifts
Explanation:
Insertion or deletion mutations (or Indel mutations) can be defined as mutations in DNA due to insertion (addition) or deletion of nucleotide bases in DNA.
These mutations lead to change in reading frames (sequence of codons), which leads to formation of protein having completely different amino acid sequence. Hence, these mutations are also cause frameshift mutations.
This is due due to triplet nature of genetic codes as insertion or deletion of one or more bases (but not three) would change change in codon sequence and mutated sequence can form a non-functional or truncated protein.
Thus, the correct answer is option (A).
Answer:
substantive genes
Explanation:
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Answer:
b. A transferase deficiency will result in an accumulation of the toxic metabolite galactosse 1-phosphate.
c. A galactokinase deficiency will cause an accumulation of galactose.
Explanation:
Transferase is an enzyme which is responsible for the breakdown of galactose which is a known milk sugar. Its deficiency causes the formation of toxic materials such as galactose-1-phosphate which comes from galactose, and galactitol. Galactokinase is also an enzyme which helps in the conversion of galactose into galactose 1-phosphate with the expenditure of ATP molecule, so its deficiency causes the deposition of galactose.
One organic waste that is not found in urine is called Bicarbonate Ions
