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

页码：200 / 200

页数：1

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