Hyperhomocysteinemia is common in sickle cell disease but is not explained by folate or cobalamin deficiency.

被引：0
|
作者：
Dhar, M
Bellevue, R
Brar, S
Ashrafzadeh, A
Carmel, R
机构：
[1] New York Methodist Hosp, Dept Med, Brooklyn, NY USA
[2] New York Methodist Hosp, Comprehens Sickle Cell Thalassemia Program, Brooklyn, NY USA
[3] Cornell Univ, Weill Med Coll, Dept Med, New York, NY USA
来源：
BLOOD | 2001年 / 98卷 / 11期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
2046
引用
收藏
页码：490A / 491A
页数：2
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