Human Molecular Genetics Advance Access originally published online on November 12, 2007
Human Molecular Genetics 2008 17(1):158; doi:10.1093/hmg/ddm313
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MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor1 and angiotensin II
Human Molecular Genetics (2007) 16;20, pp. 2453–2462; doi:10.1093/hmg/ddm201
The authors would like to apologise for an error in the Acknowledgements. The text reads S.R. is a few scholar but should read C.S.R is a Pew Scholar. The corrected Acknowledgements section is reproduced below.
ACKNOWLEDGEMENTS
We would like to thank the patients and their families for participating in these studies. We are indebted to Dr Sudha Veeraraghavan for help with generating the structure panels and to Dr Jeunemaitre and Dr Zhu at the Assistance Publique Hopitaux de Paris for sharing information about polymorphisms in MYH11. C.S.R. is a Pew Scholar. D.M.M. is a Doris Duke Distinguished Clinical Scientist.
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