Výsledky vyhledávání - "Christopher B. Merrick"

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14

Autor: Tom G. W. Letteboer, David A. Quigley, Michael Benzinou, Rosemary J. Akhurst, C.J.J. Westermann, Jonathan H. Berg, Il-Jin Kim, Allan Balmain, S. Giraud, Johannes Kristian Ploos Van Amstel, David M. Jablons, Christopher B. Merrick, Gaetan Lesca, Minh D. To, Kechen Zhau, Sophie Dupuis-Girod

Publikováno v: Frontiers in Genetics [E], 5(FEB). Frontiers Media S. A.
Frontiers in Genetics

HHT shows clinical variability within and between families. Organ site and prevalence of arteriovenous malformations (AVMs) depend on the HHT causative gene and on environmental and genetic modifiers. We tested whether variation in the functional ENG

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01a7b642b4763692917145569292dbe5

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