FHLdb: A Comprehensive Database on the Molecular Basis of Familial Hemophagocytic Lymphohistiocytosis

Background: Primary immunodeficiencies (PIDs) are a heterogeneous group of disorders. The lack of comprehensive disease-specific mutation databases may hinder or delay classification of the genetic variants found in samples from these patients. This is especially true for familial hemophagocytic lym...

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Detalles Bibliográficos
Autores principales: Viñas-Giménez, Laura, Padilla, Natàlia, Batlle-Masó, Laura, Casals, Ferran, Rivière, Jacques G., Martínez-Gallo, Mónica, de la Cruz, Xavier, Colobran, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006814/
https://www.ncbi.nlm.nih.gov/pubmed/32076423
http://dx.doi.org/10.3389/fimmu.2020.00107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006814/
https://www.ncbi.nlm.nih.gov/pubmed/32076423
http://dx.doi.org/10.3389/fimmu.2020.00107

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