A frameshift mutation in a gene refers to the insertion or deletion of nucleotide bases in numbers that are not multiples of three. |
A frameshift mutation is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by ... |
A frameshift mutation is a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read. |
Frameshift mutation refers to the addition or deletion of nucleotides that alters the reading frame of the ribosome during translation, resulting in ... |
An insertion or deletion involving a number of base pairs that is not a multiple of three, which consequently disrupts the triplet reading frame of a DNA ... |
Frameshift mutations are deletions or additions of 1, 2, or 4 nucleotides that change the ribosome reading frame and cause premature termination of translation ... |
Frame-shift mutations. This means that when the groups of three nucleotides (codons) are read at the ribosome, the codon reading frame is shifted by one codon. |
A type of mutation in which a number of NUCLEOTIDES deleted from or inserted into a protein coding sequence is not divisible by three, thereby causing an ... |
A frameshift mutation is an insertion or deletion mutation that affects the reading frame of the gene, resulting in large numbers of altered amino acids. |
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