Truncation of Ube3a-ATS Unsilences Paternal Ube3a and Ameliorates Behavioral Defects in the Angelman Syndrome Mouse Model
Linyan Meng(Baylor Genetics), Arthur L. Beaudet(Lunar and Planetary Institute), Mauro Costa‐Mattioli(Bay Institute), Wei Huang(Sichuan University), Ping Zhu(Baylor College of Medicine), Richard Person(GenVec)
Cited by 170
Related Papers
The NIH Roadmap Epigenomics Mapping Consortium
|Nature Biotechnology|2010|2k
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
|Nature Genetics|1993|1.7k
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
|Neuron|2015|1.5k
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
|New England Journal of Medicine|2012|1.4k