The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders-Reference-Cited by-同舟云学术

The role of translation elongation factor eEF1 subunits in neurodevelopmental disorders

Published:2018-11-23 Issue:2 Volume:40 Page:131-141
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

McLachlan Fiona¹,Sires Anna Martinez¹,Abbott Catherine M.¹^ORCID

Affiliation:

1. Centre for Genomic and Experimental Medicine; Institute of Genetics and Molecular Medicine; The University of Edinburgh; Western General Hospital; Crewe Road Edinburgh UK

Funder

Medical Research Council

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.23677/fullpdf

Reference94 articles.

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4. Isolation and characterization of the rat chromosomal gene for a polypeptide (pS1) antigenically related to statin;Ann;Journal of Biological Chemistry,1991

5. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V;Antonellis;American Journal of Human Genetics,2003

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