PD linked mutation may cause neurodegeneration via different mechanism.
<h3>What is Novel Parkinson's disease linked mutation ?</h3>
A novel mutation in the α-Synuclein (α-Syn) gene "G51D" was recently identified in two familial cases exhibiting features of Parkinson's disease (PD) and multiple system atrophy (MSA)
- the G51D mutation significantly attenuates α-Syn aggregation in vitro.
- it disrupts local helix formation in the presence of SDS, decreases binding to lipid vesicles C-terminal to the site of mutation and severely inhibits helical folding in the presence of acidic vesicles.
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Answer: a. rna interference.
Rna interference <span> was known by other
names like <span>co-suppression because
it </span>has become evident that RNAi has immense potential in inhibiting desired
genes by neutralizing targeted mRNA molecules</span> Two types of small ribonucleic acid (RNA) molecules that are central to RNA interference
are miRNA and <span>siRNA. </span>
The inheritance of a dominant gene E results in the free out unattached earlobe. If the lobe is attached directly to the head, the individual is homozygous recessive, and the rest genotype is present. Hope this helps.
The answer would be Oxygen