A father with myotonic dystrophy has three daughters who are all carriers of the mutant allele and two sons who are unaffected noncarriers. the three daughters have six sons, of which four are affected and two are not, and four daughters, of which two are carriers and two are not. From this description, what type of mutation is probably responsible for myotonic dystrophy?

Inherited Autosomal Dominant Mutations

Explanation:

The mutations in DMPK gene or ZNF9 gene contribute to the onset of Muscular Dystrophy. This is a type of inherited disorder that can run in families and due to it's autosomal transfer nature, it affects both sexes equally.

answer; i believe the correct answer is (data); /// good luck

the relative standard reduction potential of the half-cell in which reduction occurs; more positive than the other half-cell. reduction is a chemical process in which electrons are added to an atom or an ion; it always occurs accompanied by oxidation of the reducing agent.