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J-GLOBAL ID:201702241855353421   Reference number:17A0283925

WDR62/MCPH2 mutations identified in patients with primary microcephaly by a combined approach of exome sequencing and genome editing technology

エキソームシークエンシングとゲノム編集技術の併用アプローチにより原発性小頭症患者において同定されたWDR62/MCPH2突然変異
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Material:
Volume: 61st(Web)  Page: ROMBUNNO.Tue(3)-P-101 (WEB ONLY)  Publication year: 2016 
JST Material Number: L1204A  Document type: Proceedings
Article type: 短報  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Genetic variation  ,  Epidemiology  ,  Diagnostics of congenital diseases, deformities. 

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