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.
Mother is b+ and o-, and father is a+ and o-
Answer:
fast moving mountain streams which flow over rocks and waterfalls are high in oxygen due to the amount of surface area of the water that is exposed to the air.
Fast moving mountain streams are high in nutrients. Organisms have adaptations to hold on in fast moving water, resulting in a large diversity organism.
Slow moving flood plain rivers are high in oxygen due to the amount of surface area of the water that is exposed to the air.
Slow moving flood plain rivers are low in nutrients. These rivers move too slow for plant growth and other organisms to survive.
a structure in the statocyst
Answer:
Distractions is a common mistake
Explanation:
