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HOME > Endocrinol Metab > Volume 20(4); 2005 > Article
Case Report A Case Report of von Hippel-Lindau Disease Manifested in a Monozygous Twin.
Jin Woo Kim, Sang Jo Choi, Yeon Kyeong Kim, Sang Mi Ahn, Kyoung Eun Song, Sun Hye Jung, Dae Jung Kim, Yoon Sok Chung, Kwan Woo Lee, Il Jin Kim, Hio Chung Kang, Jae Gahb Park
Endocrinology and Metabolism 2005;20(4):395-400
DOI: https://doi.org/10.3803/jkes.2005.20.4.395
Published online: August 1, 2005
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1Department of Endocrinology and Metaboilsm, Ajou University School of Medicine, Korea.
2Korean Hereditary Tumor Registry, Cancer Research Institute, Seoul National University College of Medicine, Korea.
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  • Germline mutation of Glu70Lys is highly frequent in Korean patients with von Hippel–Lindau (VHL) disease
    Sena Hwang, Cheol Ryong Ku, Ji In Lee, Kyu Yeon Hur, Myung-Shik Lee, Chul-Ho Lee, Kyo Yeon Koo, Jin-Sung Lee, Yumie Rhee
    Journal of Human Genetics.2014; 59(9): 488.     CrossRef
  • A Case of Type 1 von Hippel-Lindau (VHL) Disease associated with VHL Germline Mutation
    Jeong Hoon Seo, Jae Hong Yang, Pyoung Lak Choi, Yu Lee Kim, Young Sik Choi, Yo Han Park, Ji Ho Ko, Hio Chung Kang, IL Jin Kim, Jae Gahb Park
    Journal of Korean Endocrine Society.2006; 21(3): 239.     CrossRef
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