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							Conclusion
                                                           Duchenne muscular dystrophy
                                                        is a sex- linked recessive genetic
                                                        disease. The disease is caused by
                                                        multiple allelic variants.
                                                        However, many of the variants
                                                        are results from nonsense
                                                        mutations, often times base
                                                        substitutions in the DNA
                                                        sequence of an individual. The
                                                        substitution of DNA bases
                                                        creates stop codons that
                                                        terminate the sequence,
                                                        interfering with the function and
                                                        development of the protein.
                                                        Duchenne muscular dystrophy is
                                                        the consequence of the protein’s
                                                        inability to function properly.

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