Newborn diagnosis of pyridoxine-dependent epilepsy through a combined genetic approach

被引：0
|
作者：
Nobrega, Maria Soares [1 ]
Cerqueira, Rita [1 ]
Pitrez, Luena [1 ]
Rosmaninho Salgado, Joana Margarida [2 ]
Sa, Joaquim [1 ,2 ]
Teixeira, Marisa [1 ]
机构：
[1] Unilabs, cgc Genet, Porto, Portugal
[2] Ctr Hosp & Univ Coimbra, Coimbra, Portugal
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P07.033.A
引用
收藏
页码：437 / 437
页数：1
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