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American Journal of Human Genetics|August 12, 1999
The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27P A Leegwater, A A Könst, B Kuyt, et al.
American Journal of Human Genetics|March 20, 2001
Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cystsP A Leegwater, B Q Yuan, J van der Steen, et al.
Nature Genetics|November 13, 2001
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matterP A Leegwater, G Vermeulen, A A Könst, et al.
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