- Clinical Features and Mutations in the ENG, ACVRL1, and SMAD4 genes in Korean Patients with Hereditary Hemorrhagic Telangiectasia
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Lee ST, Kim JA, Jang SY, Kim DK, Do YS, Suh GY, Kim JW, Ki CS
- KMID: 1794409
- J Korean Med Sci.
- 2009 Feb;24(1):69-76.
- doi: 10.3346/jkms.2009.24.1.69
Hereditary hemorrhagic telangiectasia (HHT) is an inherited disorder that is characterized by abnormal communication between the arteries and veins in the skin, mucosa, and various organs. HHT has been reported... -
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- SERPINE2 Polymorphisms and Chronic Obstructive Pulmonary Disease
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Cha SI, Kang HG, Choi JE, Kim MJ, Park J, Lee WK, Kim CH, Jung TH, Park JY
- KMID: 1783142
- J Korean Med Sci.
- 2009 Dec;24(6):1119-1125.
- doi: 10.3346/jkms.2009.24.6.1119
A number of genome-wide linkage analyses have identified the 2q33.3-2q37.2 region as most likely to contain the genes that contribute to the susceptibility to chronic obstructive pulmonary disease (COPD). It... -
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