Whole exome sequencing in heritable white matter disorders in children
Publish place: 2nd International & 10th National Neurogenetic Congress,
Publish Year: 1396
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:
NGCMED10_017
تاریخ نمایه سازی: 16 تیر 1397
Abstract:
Myelin Disorders Clinic, Department of Child Neurology, Children’s Medical Center, Tehran University ofMedical Sciences, Tehran, Iran
Authors
Ali Reza Tavasoli
Myelin Disorders Clinic, Department of Child Neurology, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
Mahmoud Reza Ashrafi
Myelin Disorders Clinic, Department of Child Neurology, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran