Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future Directions

Hemophilia A (HA), a rare recessive X-linked bleeding disorder, is caused by either deficiency or dysfunction of coagulation factor VIII (FVIII) resulting from deleterious mutations in the F8 gene encoding FVIII. Over the last 4 decades, the methods aimed at determining the HA carrier status in fema...

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Detalles Bibliográficos
Autores principales: Dardik, Rima, Janczar, Szymon, Lalezari, Shadan, Avishai, Einat, Levy-Mendelovich, Sarina, Barg, Assaf Arie, Martinowitz, Uri, Babol-Pokora, Katarzyna, Mlynarski, Wojciech, Kenet, Gili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380558/
https://www.ncbi.nlm.nih.gov/pubmed/37511607
http://dx.doi.org/10.3390/ijms241411846

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380558/
https://www.ncbi.nlm.nih.gov/pubmed/37511607
http://dx.doi.org/10.3390/ijms241411846

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