HIGHLIGHTS
- who: Sophie Giraud from the , Bron, France have published the article: Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia, in the Journal: (JOURNAL)
- what: The aim of this study was to investigate the potential role of ENG and of other candidate genes belonging to the same biological pathway in the development of HAVMs. The authors investigated the role of different genetic factors in the occurrence of HAVM in HHT patients.
- how: As potential candidate modifier genes for HHT the authors selected ACVRL1 ENG and MADH4 . . .
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