Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.

Tsai L.P.Sue W.C.WUH-LIANG HWUKAI-HSIN LINWang T.R.2020-12-162020-12-1619960001-6578https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029681673&partnerID=40&md5=c377e47bbc323505957b6a4aad6b0f70https://scholars.lib.ntu.edu.tw/handle/123456789/526104Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.journal article89360122-s2.0-0029681673