Correction to: Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. (2018)
Attributed to:
Nottingham Molecular Pathology Node (NMPN) for Integrated Multi-platform Biomarker Research and Knowledge Transfer
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s10048-018-0554-8
PubMed Identifier: 29992365
Publication URI: http://europepmc.org/abstract/MED/29992365
Type: Journal Article/Review
Volume: 19
Parent Publication: Neurogenetics
Issue: 4
ISSN: 1364-6745