Application of Indirect Linkage Analysis for Carrier Detection of Hemophilia A in Kurdistan Region of Iraq: Usefulness of Intron 18 BclI T>A, Intron 19 HindIII C>T, and IVS7 nt27 G>A Markers

Hemophilia A (HA) is the most common congenital X-linked coagulopathy caused by mutations in the factor VIII gene. One in 5000 to 10 000 male persons worldwide suffer from HA. It is the archetype of high-cost, low-volume disease. Therefore, identification of carriers is crucial to avoid the birth of...

Descripción completa

Detalles Bibliográficos
Autores principales: Abdulqader, Aveen M. Raouf, Rachid, Shwan, Mohammed, Ali Ibrahim, Mahmood, Sarwar Noori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714943/
https://www.ncbi.nlm.nih.gov/pubmed/31179744
http://dx.doi.org/10.1177/1076029619854545

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714943/
https://www.ncbi.nlm.nih.gov/pubmed/31179744
http://dx.doi.org/10.1177/1076029619854545

Ejemplares similares