Found: 2
Select item for more details and to access through your institution.
Haploinsufficiency of AFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 29, p. 9244, doi. 10.1523/JNEUROSCI.1532-09.2009
- By:
- Publication type:
- Article
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 11, p. 2001, doi. 10.1093/hmg/ddp124
- By:
- Publication type:
- Article