Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population

BACKGROUND & OBJECTIVE: Alpha (α) thalassemia is a hereditary disorder and is caused by deletions or mutations in globin genes. It is present in two clinically significant forms: hemoglobin Bart hydrops fetalis (Hb Bart) syndrome and hemoglobin H (HbH) disease. It is highly prevalent in South-Ea...

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Detalles Bibliográficos
Autores principales: Shahid, Saba, Nadeem, Muhammad, Zahid, Danish, Hassan, Jawad, Ansari, Saqib, Shamsi, Tahir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432714/
https://www.ncbi.nlm.nih.gov/pubmed/28523047
http://dx.doi.org/10.12669/pjms.332.11834

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432714/
https://www.ncbi.nlm.nih.gov/pubmed/28523047
http://dx.doi.org/10.12669/pjms.332.11834

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