Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India

Kishalaya Das; Prasanta Purohit; Satyabrata Meher; Siris Patel; Snehadhini Dehury

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Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India

机译：印度东部具有IVS1-5（G→C）突变和印度缺失-倒置Gγ（Aγδβ）0地中海贫血的β地中海贫血的复合杂合状态

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《Revista Brasileira de Hematologia e Hemoterapia》 |2015年第3期|共5页
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Kishalaya Das; Prasanta Purohit; Satyabrata Meher; Siris Patel; Snehadhini Dehury;
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中图分类临床医学;
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1. Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India [J] . Kishalaya Das, Prasanta Purohit, Satyabrata Meher, Revista Brasileira de Hematologia e Hemoterapia . 2015,第3期

机译：印度东部具有IVS1-5（G→C）突变和印度缺失-倒置Gγ（Aγδβ）0地中海贫血的β地中海贫血的复合杂合状态
2. Compound heterozygote of Hb DIran [HBB: c.67GC, β 22(B4) GluGln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India [J] . Pradeep Kumar, Satyabrata, Snehadhini, Hematology, Transfusion and Cell Therapy . 2018,第1期

机译：印度东部的β0地中海贫血的Hb DIran [HBB：c.67G> C，β22（B4）Glu> Gln]的复合杂合子[cds 41/42（-CTTT）]
3. A new β0-thalassemia mutation (codon 102, AACATCAC) in coexistence with a heterozygous P4.2 Nippon gene [J] . AdhiyantoC., YamashiroY., HattoriY., Hemoglobin: International Journal for Hemoglobin Research . 2013,第1a6期

机译：一个新的β0地中海贫血突变（密码102，AAC> ATCAC）与杂合P4.2 Nippon基因共存
4. Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India [O] . Snehadhini Dehury, Prasanta Purohit, Satyabrata Meher, 2015

机译：印度东部具有IVS1-5（G→C）突变和印度缺失-倒置Gγ（Aγδβ）0地中海贫血的β地中海贫血的复合杂合状态
5. Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India [O] . Dehury Snehadhini, Purohit Prasanta, Meher Satyabrata, 2015

机译：印度东部带有IVS1-5（G→C）突变和印度缺失-倒置Gγ（Aγδβ）0地中海贫血的β地中海贫血的复合杂合状态

Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)0-thalassemia in eastern India

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