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Additional file 1: of Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia

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posted on 2019-08-23, 09:55 authored by Cuibai Wei, Qi Qin, Fei Chen, Aihong Zhou, Fen Wang, Xiumei Zuo, Rong Chen, Jihui Lyu, Jianping Jia
Table S1. Genes detected relate to hereditary leukoencephalopathies disease. (DOCX 18 kb)

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Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support

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    LeukodystrophiesVanishing white matter diseaseOvarioleukodystrophyEukaryotic translation initiation factor 2BAdult-onset vanishing white matter diseaseLate-onset vanishing white matter disease

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