Letters: New Observations
A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure†‡§
Funding agencies: This work was supported by grants from the Spanish Ministry of Education and Science (SAF2007-61003, SAF2010-18586).
Relevant conflicts of interest/financial disclosures: Nothing to report.
Full financial disclosures and author roles may be found in the online version of this article.
No abstract is available for this article.