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A reply to a commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness
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نویسنده
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Yim Shin-Young ,Jeong Seon-Yong
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منبع
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journal of human genetics - 2015 - دوره : 60 - شماره : 3 - صفحه:163 -164
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آدرس
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Ajou University School of Medicine, Department of Medical Genetics, Department of Physical Medicine and Rehabilitation, South Korea, Ajou University School of Medicine, Department of Medical Genetics, South Korea
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Authors
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