References
- Jaffé E. R., Hultquist D. E. Cytochrome b5 reductase deficiency and enzymopenic hereditary methemoglobinemia. The Metabolic Basis of Inherited Disease, C. R. Scriver, A. L. Beaudet, W. S. Sly, D Valle. McGraw Hill, New York 1995; 2267–2280, 7th ed.
- Kiese M. Methemoglobinemia: a Comprehensive Treatise. CRC Press, Cleveland 1974
- Horlein H., Weber G. Uber chronische familiare Methamoglobinamie und eine neue Modifikation des Methamoglobins. Dtsch Med Wochenschr 1948; 73: 476
- Wajcman H., Leroux A. Méthémoglobinémies et sulfhémoglobinémies. Encycl Méd Chir (Elsevier, Paris) Hématologie 1998; 8, 13007 D10
- Wajcman H., Riou J., Yapo A. Globin chain analysis by reversed phase high performance liquid chromatography: recent developments. Hemoglobin 2002; 26(3)281–284
- Priest J. R., Watterson J., Jones R. T., Faassen A. E., Hedlund B. E. Mutant fetal hemoglobin causing cyanosis in a newborn. Pediatrics 1989; 83(5)734–736
- Hayashi A., Fujita T., Fujimura M., Titani K. A new abnormal fetal hemoglobin, Hb FM‐Osaka (α2γ263His→Tyr). Hemoglobin 1980; 4(3&4)447–448
- Urabe D., Li W., Hattori Y., Ohba Y. A new case of Hb F‐M‐Osaka [Gγ63(E7)His→Tyr] showed only benign neonatal cyanosis. Hemoglobin 1996; 20(2)169–173
- Glader B. E., Zwerdling D., Kutlar F., Kutlar A., Wilson J. B., Huisman T. H.J. Hb F‐M‐Osaka or α2Gγ263(E7)His→Tyr in a Caucasian male infant. Hemoglobin 1989; 13(7&8)769–773
- Hain R. D.W., Chitayat D., Cooper R., Bandler E., Eng B., Chui D. H.K., Waye J. S., Freedman M. H. Hb FM‐Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing. Hum Mutat 1994; 3(3)239–242
- Molchanova T. P., Wilson J. B., Gu L.‐H., Hain R. D.W., Chang L. S., Poon A. O., Huisman T. H.J. A second observation of the fetal methemoglobin variant Hb F‐M‐Fort Ripley or α2Gγ292(F8)His→Tyr. Hemoglobin 1992; 16(5)389–398