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For contributors- Two cases of familial cerebral cavernous malformation caused by mutations in the
CCM1 gene - Im-Yong Yang, Mi-Sun Yum, Eun-Hee Kim et al.
- Clin Exp Pediatr. 2016;59(6):280-284.
- Magnetic resonance imaging and spectroscopic analysis in 5 cases of Pelizaeus-Merzbacher disease: metabolic abnormalities as diagnostic tools
- Eun Lee, Mi-Sun Yum, Hae-Won Choi et al.
- Clin Exp Pediatr. 2012;55(10):397-402.