MOLECULAR DIAGNOSIS OF BARTH SYNDROME FIRST CASE REPORT FROM INDIA

被引：0
|
作者：
Bijarnia-Mahay, S. [1 ]
Borkar, M. [1 ]
Kotecha, U. [1 ]
Saxena, R. [1 ]
Verma, I. C. [1 ]
机构：
[1] Sir Ganga Ram Hospit, Ctr Med Genet, New Delhi, India
来源：
JOURNAL OF INHERITED METABOLIC DISEASE | 2012年 / 35卷
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D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：S59 / S59
页数：1
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