Thalassemias
Human Genetics Research Article
Characterization of molecular hemoglobin c and beta thalassemia
Authors: M.H. Lagares, M.S. Rabelo, C.G.B. Dias-penna, R.S. Mascarenhas, K.S.F. Silva and K.K.V.O. Moura
The hemoglobinopathies are a group of hereditary alterations prevalent in many parts of the world, but significantly affect the Brazilian population for its abundant miscegenation. These alterations in structural genes that cause the formation of hemoglobin variants, and/or regulatory genes, causing thalassemias. Currently, th.. Read More»
- Genet. Mol. Res. 16(4):
- gmr16039851
- DOI:
- 10.4238/gmr16039851