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Progressive ataxia associated with ocular apraxia type 1 (AOA1) with a presence of a novel mutation on the aprataxin gene
Rana, AbdulQayyum, Khan, OsamaA, Akthar, RazaVolume:
16
Year:
2013
Language:
english
Journal:
Annals of Indian Academy of Neurology
DOI:
10.4103/0972-2327.112495
File:
PDF, 805 KB
english, 2013