📣 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.

Deletion of chromosome 12q21 affecting KCNC2 and ATXN7L3B in a family with neurodevelopmental delay and ataxia. (2013)

First Author: Rajakulendran S
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jnnp-2012-304555

PubMed Identifier: 23475819

Publication URI: http://europepmc.org/abstract/MED/23475819

Type: Journal Article/Review

Volume: 84

Parent Publication: Journal of neurology, neurosurgery, and psychiatry

Issue: 11

ISSN: 0022-3050