TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed.
作者： Alessandro D. Mori , Benoit G. Bruneau
DOI: 10.1097/00001573-200405000-00004
关键词:
摘要: Purpose of reviewMutations in the T-box transcription factor TBX5 cause Holt-Oram syndrome (HOS), an autosomal-dominant condition characterized by a familial history congenital heart defects and preaxial radial ray upper limb defects. This review summarizes recent developments study TBX
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