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HOME > Endocrinol Metab > Volume 22(6); 2007 > Article
Case Report A Family of Multiple Endocrine Neoplasia Type 2A with a C634R Mutation and a G691S Polymorphism in RET Proto-oncogene.
Seoung Wook Yun, Won Sang Yoo, Koo Hyun Hong, Bae Hwan Kim, Min Ho Kang, Young Kwang Choo, Hee Yoon Park, Do Hee Kim, Hyun Kyung Chung, Myung Chul Chang, Mi Seon Kwon, Hee Jin Kim
Endocrinology and Metabolism 2007;22(6):453-459
DOI: https://doi.org/10.3803/jkes.2007.22.6.453
Published online: December 1, 2007
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1Department of Internal Medicine, College of Medicine, Dankook University, Korea.
2Department of Surgery, College of Medicine, Dankook University, Korea.
3Department of Pathology, College of Medicine, Dankook University, Korea.
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  • A Family Presenting with Catastrophic Features due to Pheochromocytoma Associated with Multiple Endocrine Neoplasia 2A
    Yun Jung Lee, Suk Chon, Sang-Ho Lee, Tae-Won Lee, Chun-Gyoo Ihm, Tae June Noh, Seungjoon Oh, Jeong-Taek Woo, Sung-Woon Kim, Jin-Woo Kim, Young Seol Kim
    Endocrinology and Metabolism.2010; 25(2): 135.     CrossRef
  • A Case of Sporadic Medullary Thyroid Cancer with RET G691S Polymorphism
    Min-Kyu Kang, Jung-Min Lee, Ji-Hyun Kim, Min-Young Lee, Ji Hyun Kim, Sung Dae Moon, Je-Ho Han, Sang-Ah Chang
    Journal of Korean Endocrine Society.2009; 24(4): 293.     CrossRef
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