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Charcot-Marie-Tooth is a muscular wasting disease that affects 1 in 2,500 people. Researchers have discovered that this occurs when a large gene on the short arm (p-arm) of chromosome number 17 makes a new copy of itself. What kind of chromosomal mutation is this?

User Glutinous
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Final answer:

Charcot-Marie-Tooth disease involves a duplication mutation on the short arm of chromosome 17, causing the gene to make an extra copy of itself.

Step-by-step explanation:

The type of chromosomal mutation described for Charcot-Marie-Tooth disease, where a large gene on the short arm (p-arm) of chromosome number 17 makes a new copy of itself, is known as duplication. This type of mutation occurs when a segment of a chromosome is copied and inserted back into the genome, leading to extra copies of genetic material. Such duplications can disrupt the normal function of genes and lead to genetic disorders.

User Shubham Shaw
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