C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome

Autor: Gröbner, Rebekka, Kapferer-Seebacher, Ines, Amberger, Albert, Redolfi, Rita, Dalonneau, Fabien, Björck, Erik, Milnes, Di, Bally, Isabelle, Rossi, Véronique, Thielens, Nicole, Stoiber, Heribert, Gaboriaud, Christine, Zschocke, Johannes

Publikováno v: Frontiers in Immunology
Frontiers in Immunology, Frontiers, 2019, 10, pp.2537. ⟨10.3389/fimmu.2019.02537⟩
Frontiers in Immunology, Frontiers, 2019, 10, ⟨10.3389/fimmu.2019.02537⟩
Frontiers in Immunology, 2019, 10, pp.2537. ⟨10.3389/fimmu.2019.02537⟩

Heterozygous missense or in-frame insertion/deletion mutations in complement 1 subunits C1r and C1s cause periodontal Ehlers-Danlos Syndrome (pEDS), a specific EDS subtype characterized by early severe periodontal destruction and connective tissue ab

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5d0afefec0b9cc03176f34665dd52da8
https://hal.archives-ouvertes.fr/hal-02351714

Corrigendum: C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome.

Autor: Gröbner, Rebekka, Kapferer-Seebacher, Ines, Amberger, Albert, Redolfi, Rita, Dalonneau, Fabien, Björck, Erik, Milnes, Di, Bally, Isabelle, Rossi, Veronique, Thielens, Nicole, Stoiber, Heribert, Gaboriaud, Christine, Zschocke, Johannes

Publikováno v: Frontiers in Immunology; 12/4/2019, Vol. 10, p1-1, 1p