Novel Βeta (β)-Thalassemia Mutation in Turkish Children

Beta (β)-thalassemia is the most frequently observed hereditary blood disorder in the world. It is characterized by deficiency of hemoglobin β-globin gene and is also a profoundly heterogeneous both at the molecular and clinical level. In the case of β-thalassemia, there is reduced (β(+) type) or ab...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Indian J Hematol Blood Transfus
मुख्य लेखकों: Ulasli, Mustafa, Oztuzcu, Serdar, Kirkbes, Sevil, Bay, Ali, Igci, Yusuf Ziya, Bayraktar, Recep, Igci, Mehri, Ergun, Sercan, Cakmak, Ecir Ali, Aytekin, Elif, Arslan, Ahmet
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Springer India 2014
विषय:
Original Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4375154/
https://ncbi.nlm.nih.gov/pubmed/25825561
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0380-6
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