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<p>disorders occur in individuals who have <a href="page.php?w=homozygous">two copies of an allele</a> for a particular recessive genetic <a href="page.php?w=mutation">mutation</a>. Except in certain rare circumstances, such as new mutations or <a href="page.php?w=uniparental_disomy">uniparental disomy</a>, both parents of an individual with such a disorder will be carriers of the gene. These carriers do not display any signs of the mutation and may be unaware that they carry the mutated gene. Since relatives share a higher proportion of their genes</p><p>
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