Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases. (2012)

First Author: Sailer A

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/WNL.0b013e31825f048e

PubMed Identifier: 22675081

Publication URI: http://europepmc.org/abstract/MED/22675081

Type: Journal Article/Review

Volume: 79

Parent Publication: Neurology

Issue: 2

ISSN: 0028-3878