These authors contributed equally to this work.
Article first published online: 1 DEC 2011
Copyright © 2011 Wiley Periodicals, Inc.
Birth Defects Research Part A: Clinical and Molecular Teratology
Volume 94, Issue 1, pages 47–51, January 2012
How to Cite
Leon, T. Y.Y., So, M.-T., Lui, V. C.H., Hofstra, R. M.W., Tam, P. K.H., Ngan, E. S.W. and Garcia-Barceló, M.-M. (2012), Functional analyses of RET mutations in Chinese hirschsprung disease patients. Birth Defects Research Part A: Clinical and Molecular Teratology, 94: 47–51. doi: 10.1002/bdra.22863
This work was supported by research grants from the Hong Kong Research Grants Council (765407M) and the University of Hong Kong Seed Funding Programme for Basic Research to Maria-Mercè Garcia–Barcelo.
- Issue published online: 10 JAN 2012
- Article first published online: 1 DEC 2011
- Manuscript Accepted: 25 AUG 2011
- Manuscript Revised: 17 AUG 2011
- Manuscript Received: 13 JUL 2011
Additional Supporting Information may be found in the online version of this article.
|BDRA_22863_sm_Tables.doc||99K||Supplementary Table 1 Primers for site-directed mutagenesis PCR. Primers were designed from reference sequence (NM020630). Supplementary Table 2 Sequencing primers of the mutant constructs. Primers were designed from reference sequence (NM020630) and pcDNA3.1. Supplementary Table 3 Antibodies used in the current study.|
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