EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report
Abstract Background Leukoencephalopathy with vanishing white matter (VWM) is an autosomal recessive neurological disease. The physiopathology of disease is still little understood, but it seems to involve impairment in maturation of astrocytes; as a consequence white matter is more prone to cellular...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
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BMC,
2022-07-01T00:00:00Z.
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