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[The coding region of WT1 gene was screened in 384 patients with POF and 6 novel variations were identified, including two missense mutations (p. Pro126Ser in exon1 and p. Arg370His in exon7) and four intronic variants (c.647-27C?>?T, c.647-13G?>?C, c.647-13G?>?A in intron1 and c.950?+?14T?>?C in intron 4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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