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A de novo truncating mutation in ASXL1 associated with segmental overgrowth. (2019)

First Author: Efthymiou S

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s12041-019-1155-5

PubMed Identifier: 31819025

Publication URI: http://europepmc.org/abstract/MED/31819025

Type: Journal Article/Review

Volume: 98

Parent Publication: Journal of genetics

ISSN: 0022-1333