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[Five novel mutations, L88X, P161HfsX167, F270S, D506N and E720D, in the OCRL1 gene, which have not previously been reported in patients with Dent's or Lowe disease, were identified among 11 patients with the classical Dent's disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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