PKU (phenylketonuria) is a point mutation, specifically an autosomal recessive genetic disorder caused by a mutation in the PAH gene. This mutation leads to impaired metabolism of the amino acid phenylalanine. It is not a frameshift mutation, which would involve an insertion or deletion of nucleotides, shifting the reading frame of the gene.
A mutation
point mutation
choromosome mutaion
If you are looking for the term of this mutation, then the answer is point mutation.
PKU (phenylketonuria) is a point mutation, specifically an autosomal recessive genetic disorder caused by a mutation in the PAH gene. This mutation leads to impaired metabolism of the amino acid phenylalanine. It is not a frameshift mutation, which would involve an insertion or deletion of nucleotides, shifting the reading frame of the gene.
The best treatment of phenylketonuria is a diet that is extremely low in phenylalanine during childhood. A person can also take fish oil supplements and iron supplements to help treat some of the symptoms.
A mutation
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
No
point mutation
point! good luck
phenylketonuria
the correct answer is C. a substitution i know this cause i have this book to this question and point mutation is not one of the answer and i found the answer in the book -No its substituton you jack wagon your books wrong
Sorry to burst the persons bubble that said frameshift mutation but its wrong. Point mutation-gene mutation involving changes in one or a few nucleotides. point mutation
phenylketonuria
One type of dwarfism that is a point mutation is achondroplasia.