Search Results - "Tuğra Karaarslan, Fatma"

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    Two cases of early-onset autosomal recessive spastic ataxia of Charlevoix-Saguenay diagnosed in adulthood by Sahin, Turgut, Karaarslan, Fatma Tugra, Yilmaz, Rezzak, Tekgül, Şeyma, Başak, Ayşe Nazlı, Akbostanci, Muhittin Cenk

    Published in Clinical neurology and neurosurgery (01-02-2021)
    “…•ARSACS is a hereditary disorder caused by mutations in SACS gene on 13q12.•A number of SACS gene mutations have been discovered with WES.•When and whom to get…”
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    Journal Article
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