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[These data, together with fluorescence in situ hybridization analysis, demonstrated that the two siblings with XP as well as the CS patient were homozygous for the same CSB mutated allele, containing a silent C2830T change and a nonsense mutation C2282T converting Arg735 to a stop codon.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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