I believe the answer is d
Well, what do you need help with?
Answer:
(c) Inherited a mutation in a gene required for mismatch repair
Explanation:
Gene mutations are occasional changes that occur in genes, that is, the procedure by which a gene undergoes a structural change. Mutations involve the addition, deletion or substitution of one or a few nucleotides of the DNA strand. Mutation provides the emergence of new forms of a gene and, consequently, is responsible for gene variability.
It is common for several members of the same family to have the same genetic mutations, as the gene affected by the mutation may condition a trait that DNA cannot repair. An example of this is the family shown in the question above, where several people were diagnosed with the same type of cancer while still young. What probably happened in this family was that people diagnosed with cancer inherited a mutation in a gene needed to repair incompatibility.
Answer:
There are five basic modes of inheritance for single-gene diseases: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive, and mitochondrial. Genetic heterogeneity is a common phenomenon with both single-gene diseases and complex multi-factorial diseases
The plasma membrane has a double layer of phospholipids with proteins dispersed throughout. These proteins help increase the durability of the membrane, as well as help with filtration.
