Ataxia with ocular apraxia type 2 not responding to 4-aminopyridine: A rare mutation in the SETX gene in a Saudi patient

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Bibliographic Details
Published in:Intractable & rare diseases research 2018, Vol.7 (4), p.275-279
Main Authors: Algahtani, Hussein, Shirah, Bader, Algahtani, Raghad, Naseer, Muhammad Imran, Al-Qahtani, Mohammad H, Abdulkareem, Angham Abdulrahman
Format: Report
Language:English
Online Access:Get full text
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ISSN:2186-3644
DOI:10.5582/irdr.2018.01107