📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance (2013)

First Author: Sumner C

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.10.006

PubMed Identifier: 24207122

Publication URI: http://europepmc.org/abstract/MED/24207122

Type: Journal Article/Review

Parent Publication: The American Journal of Human Genetics

Issue: 5

ISSN: 0002-9297