Factor VII deficiency: a novel missense variant and genotype–phenotype correlation in patients from Southern Italy

This study aimed at attempting to correlate genotype and phenotype in factor VII deficiency. Here, we present molecular and clinical findings of 10 patients with factor VII deficiency. From 2013 to 2016, 10 subjects were referred to our center because of a prolonged prothrombin time identified durin...

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Detalles Bibliográficos
Autores principales: Tiscia, Giovanni, Favuzzi, Giovanni, Chinni, Elena, Colaizzo, Donatella, Fischetti, Lucia, Intrieri, Mariano, Margaglione, Maurizio, Grandone, Elvira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667183/
https://www.ncbi.nlm.nih.gov/pubmed/29104756
http://dx.doi.org/10.1038/hgv.2017.48

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667183/
https://www.ncbi.nlm.nih.gov/pubmed/29104756
http://dx.doi.org/10.1038/hgv.2017.48

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