Answer: <em>D. Causes an accumulation of lipids in brain cells</em>
Explanation:
Tay-Sachs disease is caused by a genetic mutation in the <em>HEXA</em> gene. It is an autosomal recessive disease that causes the mutation on an enzyme, which metabolizes <em>GM2 Ganglioside</em> in nerve cells, this leads to a build-up of the molecule in brain cells. At the moment there is no cure for the disease, only support treatment is available.
New media, smaller equipment, and instant sharing, are all part of the new environmentalist tools for visual documentation.
<h3>What is Visual documentation?</h3>
This is defined as the process in which knowledge or information is managed and organized in a visual manner.
This however employs the use of equipment such as projectors and internet sharing devices to ensure that the information is disseminated to a large number of people.
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Explanation:
Where Translation Occurs. Within all cells, the translation machinery resides within a specialized organelle called the ribosome. In eukaryotes, mature mRNA molecules must leave the nucleus and travel to the cytoplasm, where the ribosomes are located.
Explanation:
<u>C. A red allele is present on both homologous chromosomes</u>
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Homologous chromosomes are pairs of chromosome of similar lengths, banding patterns, and centromere positions, with genes at the same loci. For dominance, gene copies are present on both of the chromosomes; the dominat variant overrides the effect of the other recessive allele.
Further Explanation:
DNA molecules contain chromosomes that may have different forms called alleles. DNA, which is the genotype, is transcribed into mRNA and later translated into amino acids which are connected together by rRNA to form proteins which constitute the phenotype of an organism. DNA sequence mutations form new alleles, impacting the associated mRNA, and thus the encoded protein.
Homozygous individuals have a chromosome containing two variants of the same allele. Dominant homozygous individuals bear two copies of the dominant allele, whereas recessive homozygous individuals hold two copies of the recessive allele.
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B is the answer if not B then C
