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Correction to: Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. (2018)

First Author: Caylor RC

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