Publication | Open Access
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease
26
Citations
11
References
2009
Year
EngineeringAutoimmune DiseaseDisease MechanismGenetic DisorderMedicineMendelian DisorderPathogenesisGenetic EpidemiologyPathologyComplex DiseaseOmicsWhite Matter DiseaseNovel Eif2b MutationsDisease Gene IdentificationSystems BiologyMolecular DiagnosticsChinese Patients
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