Answer:True
Explanation:I cannot remember the exact details, but his is definitely a question on a food service card test, and it is definitely true.
Answer:
Una deficiencia de fósforo puede causar inapetencia, anemia (recuento bajo de glóbulos rojos), debilidad muscular, problemas de coordinación, dolor óseo, huesos blandos y deformados, un mayor riesgo de infección, una sensación de ardor o picazón en la piel y confusión.
Explanation:
espero y te sirva
Answer:
Explanation:
The photoelectric effect is a phenomenon in which electrons are emitted from matter (metals and non-metallic solids, liquids, or gases) after the absorption of energy from electromagnetic radiation such as visible light. One example of the photoelectric effect of light can be seen with zinc
A mutation within a gene that will insert a untimely cease codon in mRNA would result in a shortened polypeptide chain.
<h3>What occurs if there is a untimely end codon?</h3>
Thus, nonsense mutations occur when a premature nonsense or end codon is added in the DNA sequence. When the mutated sequence is translated into a protein, the resulting protein is incomplete and shorter than normal. Consequently, most nonsense mutations result in nonfunctional proteins
<h3>What mutation motives untimely cease codon?</h3>
In genetics, a nonsense mutation is a factor mutation in a sequence of DNA that effects in a premature stop codon, or a nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and normally nonfunctional protein product.
Learn more about mutation here:
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brainly.com/question/17031191</h3><h3 /><h3>#SPJ4</h3>
Answer:
Women who carry one copy of the mutated gene still have normal color vision because they have another copy, which is not mutated, in the other X chromosome that will be the dominant one. As a result, the women are carriers of the mutated gene but not color blind.
Explanation:
Colorblindness is a sex-linked mutation. A woman has two X chromosomes, while a man has one X chromosome and one Y chromosome. The mutated gene that causes color blindness is on the X chromosome, and it is OPN1LW. So if a woman has one mutated OPN1LW in one of her two X chromosomes, the OPN1LW gene in the other X chromosome will be the dominant one stopping the woman from being colorblind.
In the case of men, as they only have one X chromosome, if there is a mutation on the OPN1LW in the X chromosome, the men will be colorblind because there is no extra copy of the gene, as it is in women.
