Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia. (2013)

First Author: Oates EC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.04.018

PubMed Identifier: 23664120

Publication URI: http://europepmc.org/abstract/MED/23664120

Type: Journal Article/Review

Volume: 92

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297