Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
Answer: b. one atom transfers an electron to another atom
Explanation:
An ionic bond is also called as the electrovalent bond. It is a type of linkage that is formed by the electrostatic attraction formed between ions of opposite charge in a chemical compound.
These bonds are formed when the valence electrons from one of the atom are transferred to the another atom.
The region that would be eroded the most would be those at the slopes of the mountain. When heavy rainfall comes, the soil in these regions gets soften thus being forced down forming a run-off due to the force of gravity. These eroded soil would eventually continue to the valleys thus causing landslides.
Answer:
Because it help us to maintain biodiversity of our planet.
Explanation:
