Abstract
Investigators from Massachusetts General Hospital, Boston, and centers in Frankfurt, Germany, examined 22 patients with the classic phenotype of ataxia-telangiectasia for neurocognitive features, and compared patients with early stage cerebellar disease (group AT-I) versus those with late stage cerebrocerebellar disease (group AT-II).
DOI: https://doi.org/10.15844/pedneurbriefs-28-11-2 | Journal eISSN: 2166-6482
Language: English
Page range: 82 - 83
Published on: Nov 1, 2014
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.