Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype

被引：12

作者：

Italia, Khushnooma ^{[1
]}

Kangne, Harshada ^{[1
]}

Shanmukaiah, Chandrakala ^{[2
]}

Nadkarni, Anita H. ^{[1
]}

Ghosh, Kanjaksha ^{[1
]}

Colah, Roshan B. ^{[1
]}

机构：

[1] King Edward Mem Hosp, Natl Inst Immunohaematol, Bombay, Maharashtra, India

[2] King Edward Mem Hosp, Dept Haematol, Bombay, Maharashtra, India

来源：

BRITISH JOURNAL OF HAEMATOLOGY | 2015年 / 168卷 / 01期

关键词：

sickle cell disease; genetic modifiers; vaso-occlusive crisis; stroke; MTHFR; ANEMIA; GENE;

D O I：

10.1111/bjh.13083

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：156 / 159

页数：4

共 11 条

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[J]. BRITISH JOURNAL OF HAEMATOLOGY, 2014, 164 (04) : 597 - 604
[3] Sickle cell disease in India
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[J]. CURRENT OPINION IN HEMATOLOGY, 2014, 21 (03) : 215 - 223
[4] Hydroxyurea in sickle cell disease-A study of clinico-pharmacological efficacy in the Indian haplotype
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[J]. BLOOD CELLS MOLECULES AND DISEASES, 2009, 42 (01) : 25 - 31
[5] Sickle cell anemia from central India: A retrospective analysis
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[J]. INDIAN PEDIATRICS, 2012, 49 (11) : 911 - 913
[6] KAR BC, 1986, LANCET, V2, P1198
[7] Sickle cell disease: A multigenic perspective of a single gene disorder
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[J]. HEMOGLOBIN, 2007, 31 (02) : 209 - 224
[8] Mukherjee MB, 1997, AM J HEMATOL, V55, P104, DOI 10.1002/(SICI)1096-8652(199706)55:2<104::AID-AJH9>3.0.CO
[9] 2-X
[10] Fetal hemoglobin in sickle cell anemia: a glass half full?
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[J]. BLOOD, 2014, 123 (04) : 481 - 485

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