A novel mutation (4040-4045 nt. delA) in exon 14 of the factor VIII gene causing severe hemophilia A

Hemophilia A is an X-linked congenital bleeding disorder caused by Factor VIII deficiency. Different mutations including point mutations, deletions, insertions and inversions have been reported in the FVIII gene, which cause hemophilia A. In the current study, with the use of conformational sensitiv...

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Detalles Bibliográficos
Autores principales: Onsori, Habib, Feizi, Mohammad Ali Hosseinpour, Feizi, Abbas Ali Hosseinpour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276996/
https://www.ncbi.nlm.nih.gov/pubmed/22345999
http://dx.doi.org/10.4103/0971-6866.92095

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