A disease agent can affect more than one organ of the body, and more than one disease agent can affect the same organ of the body are multifactorial in origin
<h3>What is Multifactorial inheritance ?</h3>
When more than one factor contributes to a trait or health issue, such as a birth defect or persistent sickness, this is referred to as multifactorial inheritance. Genes can play a role, but other non-gene-related factors can also be important. These may consist of: Nutrition. Lifestyle
- There is general agreement that there are numerous mechanisms and reasons involved in sudden infant death syndrome, which is complex. Understanding the complex and multifaceted nature of obesity requires a study of genotype by environment interactions.
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Answer:i think its C or D
Explanation:
It cant be chemoautotrophs or photoatropus
Secondary succession happens more often because it occurs after some kind of distribution that still leaves the soil intact (mudslide,bulldozing,shoveling,or scraping off an area)
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
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1 - They all are solids due to the strong electrostatic force
<span>2 - They also have high m.p and b.p. </span>
<span>3 - It conduct electricity in molten state or in aqueous solutions </span>
