Targeted Next Generation Sequencing (NGS) identified novel mutations in rare neurodevelopmental disorders

被引：0
|
作者：
Maryam, Ammara [1 ]
Asif, Maria [2 ,3 ,4 ,5 ]
Ijaz, Muhammad [6 ]
Fatima, Urooj [6 ]
Raza, Atir [6 ]
Maheen, Nimra [6 ]
Hussain, Muhammad Sajid [3 ,7 ]
Muhammad, Farooq [6 ,8 ]
机构：
[1] Islamia Univ Bahawalpur, Inst Biochem Biotechnol & Bioinformat IBBB, Dept Biochem, Bahawalpur, Pakistan
[2] Univ Cologne, Ctr Mol Med Cologne CMMC, Cologne, Germany
[3] Univ Cologne, Fac Med, Ctr Biochem, Cologne, Germany
[4] Univ Cologne, Cologne Ctr Genom CCG, Fac Med, Cologne, Germany
[5] Univ Hosp Cologne, Cologne, Germany
[6] Islamia Univ Bahawalpur, Inst Biochem Biotechnol & Bioinformat IBBB, Dept Biotechnol, Bahawalpur, Pakistan
[7] Univ Cologne, Ctr Mol Med Cologne CMMC, Cologne, Germany
[8] Islamia Univ Bahawalpur, Inst Biochem Biotechnol & Bioinformat IBBB, Dept Bioinformat, Bahawalpur, Pakistan
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31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：
EP10.047
引用
收藏
页码：200 / 200
页数：1
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