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pro vyhledávání: '"Kerstin Mainusch"'
Autor:
Johannes Oldenburg, Zaverio M. Ruggeri, Ulrich Budde, Rainer Schwaab, Kerstin Mainusch, Tobias Obser, Jacqueline Brassard, Sonja Schneppenheim, Reinhard Schneppenheim
Publikováno v:
Blood. 97(7)
Dimerization defects of von Willebrand factor (vWF) protomers underlie von Willebrand disease (vWD) type 2A, subtype IID (vWD 2A/IID), and corresponding mutations have been identified at the 3′ end of the vWF gene in exon 52. This study identified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::778a97e28457bd3187b2dc4a49885955
https://pubmed.ncbi.nlm.nih.gov/11264172
https://pubmed.ncbi.nlm.nih.gov/11264172
