- A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg
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Lee NY, Cho HI, Kim SI, Kim BK, Ohba Y, Hattori Y
- KMID: 1421944
- J Korean Med Sci.
- 1992 Dec;7(4):385-388.
- doi: 10.3346/jkms.1992.7.4.385
We report a Korean family case of beta-thalassemia minor and Hb Queens. This is the first case report of Hb Queens in Korea. A 43-year-old male and his four... -
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- Hb Heathrow [β103(G5)Phe→Leu], a First Report in an Asian Patient with Erythrocytosis
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Shin SY, Kim HY, Kim HJ, Kim HG
- KMID: 2419129
- Yonsei Med J.
- 2017 May;58(3):665-667.
- doi: 10.3349/ymj.2017.58.3.665
Congenital erythrocytosis (CE) is a rare and heterogeneous disease. The high oxygen affinity hemoglobin (Hb) variants are the most common cause of CE. Herein, we report a Korean patient with... -
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- The First Study on Nucleotide-level Identification of Hb Koriyama in a Patient with Severe Hemolytic Anemia
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Park S, Park JE, Cho SI, Jeon Y, Park SS, Seong MW
- KMID: 1781447
- Ann Lab Med.
- 2012 Jan;32(1):99-101.
- doi: 10.3343/alm.2012.32.1.99
Hereditary hemolytic anemia comprises a group of disorders in which red blood cells are destroyed faster than they are produced in the bone marrow; various hereditary factors can cause this... -
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