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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome

Fengchang Qiao1, Chen Wang1, Chunyu Luo1

  • 1Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health care Hospital, Nanjing, China.

Molecular Genetics & Genomic Medicine
|July 27, 2019
PubMed
Abstract

Keywords:
BCL11Bdevelopmental delayintellectual disabilityneurodevelopmentwhole exome sequencing

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