**Core Concept**
Inheritance of an X-linked recessive trait involves a mutation in a gene located on the X chromosome, which can result in a condition that primarily affects males, who have only one X chromosome. Females can be carriers of the trait but typically do not express the condition themselves.

**Why the Correct Answer is Right**
Males are more likely to express X-linked recessive traits because they have only one X chromosome. If this chromosome carries the mutated gene, they will develop the condition. Females, on the other hand, have two X chromosomes, which provides a degree of protection against the expression of the trait. If a female inherits an X chromosome with the mutated gene, the other X chromosome can compensate for the affected gene, and she will not express the condition. However, she can pass the mutated gene to her offspring, increasing the likelihood of them developing the condition.

**Why Each Wrong Option is Incorrect**
* **Option A:** This option is incorrect because it does not accurately describe the inheritance pattern of an X-linked recessive trait.
* **Option B:** This option is incorrect because it suggests that females are equally likely to express X-linked recessive traits as males, which is not the case.
* **Option D:** This option is incorrect because it implies that X-linked recessive traits are inherited in an autosomal dominant pattern, which is not true.

**Clinical Pearl / High-Yield Fact**
When considering the inheritance of X-linked recessive traits, it's essential to remember that affected males will not pass the mutated gene to their sons, but all of their daughters will inherit the mutated gene and become carriers.

**Correct Answer: C.**