1 Ocak 2020 Dergi makalesi Açık Erişim

Oktay, Y.; Gungor, S.; Hiz, S.; Yaramis, A.; Aranguren-Ibanez, A.; Yis, U.; Sonmezler, E.; Yilmaz, E.; Ekinci, B.; Aslan, M.; Balaraju, S.; Szabo, N.; Laurie, S.; Beltran, S.; Hathazi, D.; MacArthur, D.; Roos, A.; Lochmuller, H.; Vernos, I.; Horvath, R.

JSON-LD (schema.org)

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      "affiliation": "Dokuz Eylul Univ, Dept Pediat Neurol, Fac Med, Izmir, Turkey", 
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      "affiliation": "Newcastle Univ, Inst Translat & Clin Res, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne, Tyne & Wear, England", 
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      "affiliation": "Univ Cambridge, Sch Clin Med, John Geest Cambridge Ctr Brain Repair, Dept Clin Neurosci, Cambridge, England", 
      "name": "Szabo, N."
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      "affiliation": "Barcelona Inst Sci & Technol, Ctr Genom Regulat, CNAG CRG, Barcelona, Spain", 
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      "affiliation": "Univ Cambridge, Sch Clin Med, John Geest Cambridge Ctr Brain Repair, Dept Clin Neurosci, Cambridge, England", 
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      "affiliation": "Univ Cambridge, Sch Clin Med, John Geest Cambridge Ctr Brain Repair, Dept Clin Neurosci, Cambridge, England", 
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  "datePublished": "2020-01-01", 
  "description": "\u00d6z bulunamad\u0131.", 
  "headline": "A homozygous missense variant inTUBGCP2alter the g-tubulin ring complex leading to abnormal cortical development, pontocerebellar atrophy and altered myelination", 
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  "name": "A homozygous missense variant inTUBGCP2alter the g-tubulin ring complex leading to abnormal cortical development, pontocerebellar atrophy and altered myelination", 
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