WHOLE EXOME SEQUENCING IN FAMILIES WITH SE-RIOUS MENTAL ILLNESSES IDENTIFIES POTENTIALLY DELETERIOUS RARE VARIANTS IN GENES IMPLICATED IN NEURODEVELOPMENT

被引：0
|
作者：
Jain, Sanjeev [1 ]
Ganesh, Suhas [2 ]
Bhattacharjee, Samsiddhi [3 ]
Vemula, Alekhya [1 ]
Nadella, Ravikumar [1 ]
Ithal, Dhruva [1 ]
Mathew, Kezia [1 ]
Viswanath, Biju [1 ]
Purushottam, Meera [1 ]
机构：
[1] Natl Inst Mental Hlth & Neurosci, Bengaluru, India
[2] Yale Univ, New Haven, CT 06520 USA
[3] Natl Inst Biomed Genom, Kalyani, W Bengal, India
来源：
EUROPEAN NEUROPSYCHOPHARMACOLOGY | 2021年 / 51卷
关键词：
D O I：
10.1016/j.euroneuro.2021.08.083
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
TU82
引用
收藏
页码：E140 / E140
页数：1
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