Correct Answer - C Ans: C. It is a trinucleotide repeat expansion type of disorder Huntington’s chorea is an autosomal dominant disorder with an increased number of CAG repeats. Clinically manifested as involuntary jerky movements, mood disturbances and finally severe dementia.
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Biochemistry Videos & Books
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9 days ago · see on TelegramCorrect Answer - C C i.e. Inhibited by ADP & activated by GTP During first few days of fasting, there is rapid breakdown of muscle protein, providing aminoacids (alanine & glutamine mainly) that are used by liver for gluconeognesisQ. In the fasting state, the output of alanine from skeleton muscle…
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