- Title
- A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene.
- Creators
- Boxun Zhao - Boston Children's HospitalJill A Madden - Boston Children's HospitalJasmine Lin - Boston Children's HospitalGerard T Berry - Boston Children's HospitalMonica H Wojcik - Harvard UniversityXuefang Zhao - Broad InstituteHarrison Brand - Broad InstituteMichael Talkowski - Broad InstituteEunjung Alice Lee - Boston Children's HospitalPankaj B Agrawal - Boston Children's Hospital
- Publication Details
- European journal of human genetics : EJHG, Vol.30(9), pp.1083-1087
- Publisher
- Springer Science and Business Media LLC; United Kingdom
- Academic Unit
- Miller School of Medicine; UMMG Dept of Pediatrics - Neonatology; UMMG Department of Pediatrics
- Resource Type
- Report
- Record Identifier
- 991031926696902976
Report
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene.
European journal of human genetics : EJHG, Vol.30(9), pp.1083-1087
Springer Science and Business Media LLC
2022
Metrics
6 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.105 Strokes
- 1.105.2272 Moyamoya Disease
- Web Of Science research areas
- Biochemistry & Molecular Biology
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites