| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8681735 | Clinical Neurology and Neurosurgery | 2018 | 4 Pages |
Abstract
The novel mutation c.1688Gâ¯>â¯A in compound heterozygous state leads to intermediate phenotype of the vanishing white matter disease. In the early stages of the disease the signal abnormality in the corpus callosum inner rim might be remarkable.
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Authors
Gonca BektaÅ, Gözde YeÅil, Melis Ulak Ãzkan, Edibe Pembegül Yıldız, TuÄçe Aksu Uzunhan, Mine ÃalıÅkan,