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.
<span>Among the following statements shown, the most accurate concerning the founder effect is that (C) </span><span>It results when a small population breakers away from a larger one. Founder Effect is defined as the reduced genetic diversity which is most likely caused </span><span>when a population is descended from a small number of colonizing ancestors.</span><span>
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I believe it's false. The nucleus is the control center of the cell. The mitochondria is commonly known as the cell's powerhouse.
Answer:
yes
Explanation:
much of Earth is currently unexplored also very little is known about Earth's past. the only things we know is what is going in fossils which are an extremely rare find
