A patient with two syndrome due to paternal uniparental disomy of chromosome 2 (pUPD2) related with homozygous novel mutations of the RAB3GAP1 and UNC80 genes

Perçin F. E., Kayhan G., Sezer A., Koç A., Ergün M. A.

Erciyes Genetik Günleri 2018 Kayseri, March 2018

• Award Scope: Award from Scientific / Professional Studies
• Award Type: Kongre, Konferans, Festival veya Sempozyum Kurullarınca Verilen Ödül
• Award Country: Turkey
• Awarding Organization: Erciyes Genetik Günleri 2018 Kayseri
• Research Areas: Health Sciences
• Award Date: March 2018