Answer:
The correct answers are "heterozygous", and "homozygous dominant".
Explanation:
Galactosemia is a condition where people are not able to process the sugar galactose. People with this condition have one gene mutated, which does not allow the proper synthesis of the enzyme that breaks down galactose. Galactosemia is inherited as an autosomal recessive genetic condition, therefore, only children that are homozygous recessive develop the condition. Children that are heterozygous or homozygous dominant, will not develop galactosemia.
Answer:d. law of universal gravitation
Explanation:
Answer:
NAD+ act both as coenzyme as well as electron acceptor compound and get reduced to NADH by accepting electron.
Explanation:
NAD+ act as co enzyme of various biological catalyst such as malate dehydrogenase, isocitrate dehydrogenase etc.
NAD+ can act as co enzyme only in its oxidized form but not in its reduced form called NADH.
Many reaction needs NAD+ to occur such as conversion of glyceraldehyde 3 phosphate to 1,3 bisphosphoglycerate, malate to oxaloacetate.
That"s why NAD+/NADH ratio is kept very high because if this ratio bychance get low then it will hamper the normal redox potential of NAD+/NADH.As a result many biochemical reaction will not take place.
The answer is, "B", "Developing country".
