A Novel Deletion Mutation of the F8 Gene for Hemophilia A

Background: Hemophilia A (HA) is an X-linked recessive blood coagulation disorder caused by a variety of abnormalities in F8 gene, resulting in the absence of impaired molecule production of factor VIII (FVIII) in the plasma. The genetic testing of the F8 gene encoding FVIII is used for confirmation...

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Detalles Bibliográficos
Autores principales: Wang, Jingwei, Gu, Jian, Chen, Hongbing, Wu, Qian, Xiong, Liang, Qiao, Bin, Zhang, Yan, Xiao, Hongjun, Tong, Yongqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689134/
https://www.ncbi.nlm.nih.gov/pubmed/36428936
http://dx.doi.org/10.3390/diagnostics12112876

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689134/
https://www.ncbi.nlm.nih.gov/pubmed/36428936
http://dx.doi.org/10.3390/diagnostics12112876

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