Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene

Title
Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene
Authors
Keywords
-
Journal
JOURNAL OF INHERITED METABOLIC DISEASE
Volume 33, Issue 6, Pages 795-802
Publisher
Springer Nature
Online
2010-09-20
DOI
10.1007/s10545-010-9196-1

Ask authors/readers for more resources

Find Funding. Review Successful Grants.

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Discover Peeref hubs

Discuss science. Find collaborators. Network.

Join a conversation