A novel homozygous mutation in ALS2 gene in four siblings with infantile-onset ascending hereditary spastic paralysis. (2014)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ejmg.2014.03.006

PubMed Identifier: 24704789

Publication URI: http://europepmc.org/abstract/MED/24704789

Type: Journal Article/Review

Volume: 57

Parent Publication: European journal of medical genetics

Issue: 6

ISSN: 1769-7212