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Rare congenital bleeding disorders

The rare congenital bleeding disorders are a heterogeneous group of diseases which include deficiencies of fibrinogen, prothrombin and factors V, V + VIII, VII, X, XI and XIII. They are usually transmitted as autosomal recessive disorders, and the prevalence of the severe forms ranges from one case...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Transl Med
Egile Nagusiak: Franchini, Massimo, Marano, Giuseppe, Pupella, Simonetta, Vaglio, Stefania, Masiello, Francesca, Veropalumbo, Eva, Piccinini, Vanessa, Pati, Ilaria, Catalano, Liviana, Liumbruno, Giancarlo Maria
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: AME Publishing Company 2018
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6174186/
https://ncbi.nlm.nih.gov/pubmed/30306070
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2018.08.34
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