Analysis of obstetric complications and uterine connective tissue in tenascin-X-deficient humans and mice

Tenascin-X (TNX) is a large, multi-domain, extracellular matrix glycoprotein. Complete deficiency of TNX in humans leads to a recessive form of Ehlers-Danlos syndrome (EDS), and TNX haploinsufficiency is a cause of hypermobility type EDS. EDS patients appear to have a higher risk of several complica...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Egging, David F., van Vlijmen-Willems, Ivonne, Choi, Jiwon, Peeters, Anita C. T. M., van Rens, Desiree, Veit, Guido, Koch, Manuel, Davis, Elaine C., Schalkwijk, Joost
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer-Verlag 2008
Aiheet:
Regular Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2386751/
https://ncbi.nlm.nih.gov/pubmed/18335242
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00441-008-0591-y
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