PRIM1 deficiency causes a distinctive primordial dwarfism syndrome. (2020)

First Author: Parry DA

Attributed to: The Scottish Genomes Partnership funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/gad.340190.120

PubMed Identifier: 33060134

Publication URI: http://europepmc.org/abstract/MED/33060134

Type: Journal Article/Review

Volume: 34

Parent Publication: Genes & development

Issue: 21-22

ISSN: 0890-9369