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:
i think its A but im not sure its because A is the best from all of them
Explanation:
The bronchi (singular: bronchus) are the airways that lead from the trachea into the lungs, and then branch into smaller bronchioles. Structurally, the bronchi are made up of cartilage that gives them stability and prevents their collapse.
Answer:
The human genome contains around 20,687 protein-coding genes. Different genes or instructions are read at different times in different cells in response to the requirements of our bodies. Each cell contains two sets of genes, one from your mother and one from your father.
Explanation:
Answer:
An active cell cycle in a child
Explanation:
