Phenomenology and disease progression of chorea-acanthocytosis patients in Spain
Author:
Funder
Advocacy for Neuroacanthocytosis Patients
ERA-net E-Rare consortium EMINA
BMBF
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference26 articles.
1. Acanthocytosis and neurological disorder without betalipoproteinemia;Critchley;Arch. Neurol.,1968
2. Autosomal recessive transmission of chorea-acanthocytosis confirmed;Danek;Acta Neuropathol.,2012
3. A conserved sorting-associated protein is mutant in chorea-acanthocytosis;Rampoldi;Nat. Genet.,2001
4. Clinical features and molecular bases of neuroacanthocytosis;Rampoldi;J. Mol. Med. Berl.,2002
5. The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis;Ueno;Nat. Genet.,2001
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