MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor1 and angiotensin II
Year: 2007
Type: article
Abstract: 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. 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.
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddm313
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W2595623665