Literature DB >> 9020376

A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T-->C)

E Mirabile, R Testa, P Samperi, C Consalvo, V Romano, G Schilirò.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1997        PMID： 9020376     DOI： 10.1111/j.1600-0609.1997.tb01412.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN： 0902-4441            Impact factor:   2.997


× No keyword cloud information.
  1 in total

1.  Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India.

Authors:  Malay B Mukherjee; Anita H Nadkarni; Ajit C Gorakshakar; Kanjaksha Ghosh; Dipika Mohanty; Roshan B Colah
Journal:  Indian J Hum Genet       Date:  2010-09
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.