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:
3.2 piles
Explanation:
step 1
Find out the number of lumps in 10 clumps
we know that
3 lumps equals 1 clump
by proportion
Let
x ----> the number of lumps
step 2
Find out how many piles are 96 lumps
we know that
10 clumps equals 1 pile
10 clumps equals 30 lumps
so
1 pile equals 30 lumps
using proportion
Let
x -----> the number of piles
Answer:
B
Explanation:
Because of the way and then you will have to get back to work
It declines. Members above will die off due to starvation, and members immediately below will proliferate and kill off (through predation) the members below themselves.
