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A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome. (2017)

First Author: Bar DZ

Attributed to: Chemical reversion of nuclear shape and other defects of Hutchinson Gilford Progeria Syndrome and Lamin A/C depleted cells funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2016-104295

PubMed Identifier: 27920058

Publication URI: http://europepmc.org/abstract/MED/27920058

Type: Journal Article/Review

Volume: 54

Parent Publication: Journal of medical genetics

Issue: 3

ISSN: 0022-2593