Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome.

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作者： Mina,Zamani ^[1] ; Tahereh,Seifi ^[2] ; Jawaher,Zeighami ^[1] ; Neda,Mazaheri ^[2] ; Emad,Jahangirnezhad ^[1] ; Minoo,Gholamzadeh ^[1] ; Alireza,Sedaghat ^[2] ; Gholamreza,Shariati ^[1] ; Hamid,Galehdari ^[1]

作者单位： Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran. ^[1] Department of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran. ^[2] Diabetes Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. ^[3] Department of Genetics, School of Medicine, Ahvaz Jundishapur University of medical Sciences, Ahvaz, Iran. ^[4]

关键词 MEGDEL SERAC1 Whole-exome sequencing rs797045105

DOI 10.32598/bcn.9.10.455

PMID 33613893

发布时间 2022-04-20

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Basic and clinical neuroscience

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Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome.

Basic and clinical neuroscience

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Basic and clinical neuroscience

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Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome.

Basic and clinical neuroscience

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Basic and clinical neuroscience

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