2 to drddfdeee shark week say hey to ask so we so so will ask week
Answer:
The correct answer is d.
Explanation:
Hydranencephaly is a rare congenital anomaly characterized by the absence and replacement of the cerebral hemispheres by cerebrospinal fluid and necrotic remains, with preservation of the membranes (leptomeninges), within a skull of normal capacity and shape. It is the most severe form of cortical destruction cerebral bilateral and is considered an extreme form of porencephaly (focal cystic cavity). It mainly affects the territory of the internal carotid artery and middle cerebral artery, with preservation of the territories supplied by the vertebrobasilar arteries. The most accepted etiology is carotid vascular insufficiency, due to multiple causes (bleeding, placental thromboembolism, arteritis, vascular malformations, among others).
The router through which water will travel inside the root is <span>Xylem --> phloem --> endodermis --> stele --> epidermis --> cortex --> cambium. The correct option among all the options that are given in the question is the second option or option "B". I hope that this is the answer you were looking for and it has helped you.</span>
Answer:
The correct answer is option b. "cause a change in the reading frame of mRNA codons".
Explanation:
Frameshift mutations are among the most drastic mutations because in most cases, result in the translation of a completely different protein. Frameshift mutations are the result of insertions or deletion of one or more nucleotides, resulting in a change in the reading frame of mRNA codons. In consequence, the ribosome translates a different amino acid sequence, based on the new reading frame of mRNA codons.
