Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Yasmin A Qomawi"'
Autor:
Rehab Y Al-Ansari, Leena M Abdalla, Yasmin A Qomawi, Laila J Alromaih, Mohanad O Bakkar, Amal S Shilash, Nawaf Y Zakary
Publikováno v:
Journal of Family and Community Medicine, Vol 29, Iss 1, Pp 71-78 (2022)
BACKGROUND: Sickle cell disease (SCD) is a group of hereditary diseases, inherited as autosomal recessive disorder, which causes mutation in the β-globin gene. As a result, there is a change in the sixth amino acid from glutamic acid to valine. The
Externí odkaz:
https://doaj.org/article/e793caba6f9d4348af35db0cba97fe0b
Autor:
Rehab Y, Al-Ansari, Leena M, Abdalla, Yasmin A, Qomawi, Laila J, Alromaih, Mohanad O, Bakkar, Amal S, Shilash, Nawaf Y, Zakary
Publikováno v:
Journal of familycommunity medicine. 29(1)
Sickle cell disease (SCD) is a group of hereditary diseases, inherited as autosomal recessive disorder, which causes mutation in the β-globin gene. As a result, there is a change in the sixth amino acid from glutamic acid to valine. The affected red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f527219be151184fb6609e65d06765e1
https://pubmed.ncbi.nlm.nih.gov/35197731
https://pubmed.ncbi.nlm.nih.gov/35197731