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Journals / Turkish Journal of Hematology / 2015 / Cilt: 32 - Sayı: 1

About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur

Şinasi ÖZSOYLU
Pages
90–91
DOI
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ÖZSOYLU, Ş. (2015). About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur. Turkish Journal of Hematology, Cilt: 32 - Sayı: 1, 90–91. https://ajindex.com/articles/413119

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References (4)

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  2. Takahara S, Hamilton HB, Neel JV, Kobara TY, Ogura Y, Nishimura ET. Hypocatalasemia: a new genetic carrier state. J Clin Invest 1960;39:610-619
  3. Akar N, Torun D, Öztürk A. Hemoglobin Lansing (alpha) [HBA2 CD87 (HIS>GLU) (C>A)] in a Turkish individual resulting from another nucleotide substitution. Turk J Hematol 2014;31:317-318
  4. Colak A, Toprak B, Yararbas K, Akyol F, Ceylan C. First observation of hemoglobin Jabalpur [beta 3 (NA3) Lac>Pro] in the Turkish population. Turk J Hematol 2014;31:319- 320.