Skip to Main Content

Paper Details

A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene.
Eur J Hum Genet
8
2022
Author NameAffiliation
Jill A MaddenBoston Children's Hospital and Harvard Medical School
Jill A MaddenManton Center for Orphan Disease Research, Boston Children's Hospital
Monica H WojcikBoston Children's Hospital and Harvard Medical School
Monica H WojcikManton Center for Orphan Disease Research, Boston Children's Hospital
Monica H WojcikThe Broad Institute of Harvard and MIT
Monica H WojcikBoston Children's Hospital and Harvard Medical School
Pankaj B AgrawalBoston Children's Hospital and Harvard Medical School
Pankaj B AgrawalManton Center for Orphan Disease Research, Boston Children's Hospital
Pankaj B AgrawalThe Broad Institute of Harvard and MIT
Pankaj B AgrawalBoston Children's Hospital and Harvard Medical School
  • 1 - 10

Datasets

Release 1.2