PubMed:11301317 / 1410-1591 JSONTXT

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{"project":"PubCasesORDO","denotations":[{"id":"AB4","span":{"begin":165,"end":180},"obj":"ORDO:782"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"These results describe the first dominant negative missense mutation in a homeodomain and support a model that may partially explain the phenotypic variation within Rieger syndrome."}

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