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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Publicado en:Hum Genome Var
Main Authors: Tiscia, Giovanni, Favuzzi, Giovanni, Chinni, Elena, Colaizzo, Donatella, Fischetti, Lucia, Intrieri, Mariano, Margaglione, Maurizio, Grandone, Elvira
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group 2017
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5667183/
https://ncbi.nlm.nih.gov/pubmed/29104756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2017.48
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