Article ID Journal Published Year Pages File Type
8315014 Clinica Chimica Acta 2012 4 Pages PDF
Abstract
► Describing a two-generation Chinese family with a variant form of mild synpolydactyly. ► An R31Q mutation was found in the HOXD13 homeodomain. ► The mutation of R31Q affected the transcriptional activation ability of HOXD13.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
Authors
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