Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5: identification of a novel mutation. Clin Res Cardiol 2006 Sep;95(9):499-503
Date
07/18/2006Pubmed ID
16845574DOI
10.1007/s00392-006-0412-9Scopus ID
2-s2.0-33748144332 (requires institutional sign-in at Scopus site) 29 CitationsAuthor List
König K, Will JC, Berger F, Müller D, Benson DWMESH terms used to index this publication - Major topics in bold
AdultGenes, Homeobox
Heart Block
Heart Defects, Congenital
Humans
Male
Mutation
Pedigree
Transcription Factors
