Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. (2010)

First Author: Di Bella D

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.544

PubMed Identifier: 20208537

Publication URI: http://europepmc.org/abstract/MED/20208537

Type: Journal Article/Review

Volume: 42

Parent Publication: Nature genetics

Issue: 4

ISSN: 1061-4036