Year: 2018
Type: editorial
Abstract: An estimated 7% of the world’s population carries a mutation for a monogenetic disorder of hemoglobin, resulting in >250 000 individuals born each year with clinically significant sickle cell disease and >300 000 born each year with thalassemia. The outlook for both disorders has improved
Source: Blood
Author: Thomas D. Coates
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W2891590988
