The reason why interdisciplinary science is important to
society is because of the following reasons; It has incorporate sources of
knowledge and it is a way of increasing our knowledge. This science has made
people realize and learn more things than they actually know and it made people
understand things around them without having to actually think an explanation
behind it.
Duchenne muyscular dystrophy is caused by a mutation on the X chromosome, so a male gets it from his mother's X, if she is a carrier. The male child gets a Y and no X from his father, so the disease is always transmitted through the X from the mother. If a female gets Duchenne muscular dystrophy she has to have two X chromosomes, one from a carrier mother and another from from an affected father. This is virtually impossible because most males die before childbearing age and there is no way a female child can get an X from a man who does not live long enough to procreate. About eight percent of carrier women do show some muscle weakness, but they do not have the disease.
Without undergoing any changes itself, the enzyme makes changes to the substrate.
<h3>What is an enzyme?</h3>
An enzyme is a biological catalyst that acts by lowering the activation energy in a chemical reaction.
In a chemical reaction, an enzyme binds to a substrate to convert it to one or more products.
In conclusion, without undergoing any changes itself, the enzyme makes changes to the substrate.
Learn more about enzymes here:
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Answer:
In strict mode, the narrow-sense heritability is the proportion of the additive genetic variance that contributes to the total of the phenotypic variance. This value can be associated with the inheritance of the a-thalassemia
.
Explanation:
A-thalassemia is a genetic disorder caused by mutations affecting four different genes that encode alpha-globin, thus affecting the hemoglobin production process and, consequently, oxygen transport. The mode of inheritance of the a-thalassemia may be associated with narrow sense heritability since the phenotype is manifested by gradation, i.e., each allele might contribute in similar mode to this genetic condition.
