Identification and characterization of novel mutations implicated in congenital fibrinogen disorders

ESSENTIALS: Fibrinogen Disorders are characterized by variable expressivity. Patients with fibrinogen disorders can present with bleeding, thrombosis, or both. As previously reported, genotype‐phenotype correlations are difficult to establish. Molecular modeling may help to further understand the ef...

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Detalles Bibliográficos
Autores principales: Smith, Natalie, Bornikova, Larissa, Noetzli, Leila, Guglielmone, Hugo, Minoldo, Salvador, Backos, Donald S., Jacobson, Linda, Thornburg, Courtney D., Escobar, Miguel, White‐Adams, Tara C., Wolberg, Alisa S., Manco‐Johnson, Marilyn, Di Paola, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles: Haemostasis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178649/
https://www.ncbi.nlm.nih.gov/pubmed/30349899
http://dx.doi.org/10.1002/rth2.12127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178649/
https://www.ncbi.nlm.nih.gov/pubmed/30349899
http://dx.doi.org/10.1002/rth2.12127

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