Correction: A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1

Detalles Bibliográficos
Autores principales: Johnsrud, Irene, Kulseth, Mari Ann, Rødningen, Olaug Kristin, Landrø, Linn, Helsing, Per, Waage Nielsen, Erik, Heimdal, Ketil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536201/
https://www.ncbi.nlm.nih.gov/pubmed/26270546
http://dx.doi.org/10.1371/journal.pone.0136011
Descripción
Sumario:

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