Whole exome sequencing in heritable white matter disorders in children

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