Common Β- Thalassaemia Mutations in
Introduction: β –Thalassaemia was first explained by Thomas Cooly as Cooly’s anaemia in 1925. The β- thalassaemias are hereditary autosomal disorders with decreased or absent β-globin chain synthesis. The most common genetic defects in β-thalassaemias are caused by point mutations, micro deletions o...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Persa |
| Publicado em: |
Shahid Sadoughi University of Medical Sciences
2005-01-01
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| coleção: | Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd |
| Assuntos: | |
| Acesso em linha: | http://85.185.157.11:6280/jssu/browse.php?a_code=A-10-1-1071&slc_lang=en&sid=1 |
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