Author:
de’Angelis Nicola,Abdalla Solafah,Carra Maria Clotilde,Lizzi Vincenzo,Martínez-Pérez Aleix,Habibi Anoosha,Bartolucci Pablo,Galactéros Frédéric,Laurent Alexis,Brunetti Francesco
Publisher
Springer Science and Business Media LLC
Reference67 articles.
1. Weatherall DJ (2010) The inherited diseases of hemoglobin are an emerging global health burden. Blood 115:4331–4336
2. Gomes E, Castetbon K, Goulet V (2015) Sickle-cell related mortality in France: age and causes of death. Bulletin Epidemiologique Hebdomadaire
3. Habibi A, Arlet JB, Stankovic K, Gellen-Dautremer J, Ribeil JA, Bartolucci P, Lionnet F, centre de reference maladies r (2015) [French guidelines for the management of adult sickle cell disease: 2015 update]. Rev Med Interne 36:5S3-84
4. Hunt JA, Ingram VM (1958) Allelomorphism and the chemical differences of the human haemoglobins A, S and C. Nature 181:1062–1063
5. Ingram VM (1956) A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin. Nature 178:792–794
Cited by
14 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献