A Case of an African American Man With Ataxia and Oculomotor Apraxia 2
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology,General Medicine
Reference5 articles.
1. . Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.;Le Ber;Brain,2004
2. . Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, gammaglobulin, and alpha-fetoprotein.;Watanabe;Ann Neurol,1998
3. . Ataxia with oculomotor apraxia type 2: clinical, biological and genotypephenotype correlation study of a cohort of 90 patients.;Anheim;Brain,2009
4. . SETX gene novel mutations in a non-French Canadian with ataxia-oculomotor apraxia type 2.;Ghrooda;Parkinsonism Relat Disord,2012
5. . SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.;Nanetti;Orphanet J Rare Dis,2013
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