Hb F-LA grange or α2γ2101(G3)Glu → Lys; 75IIe; 136Gly: A high affinity fetal hemoglobin variant observed in a caucasian newborn

Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular

Volumn 789, Issue 2, 1984, Pages 224-228

  Nakatsuji, T ^a   Shimizu, K ^a   Huisman, T H J ^a  

^a Division of Hematology/Oncology   (United States)

Author keywords

(Human, fetal); Hemoglobin; Oxygen affinity; Protein stability; chain

Indexed keywords

HEMOGLOBIN F; HEMOGLOBIN VARIANT;

AMINO ACID SUBSTITUTION; BLOOD AND HEMOPOIETIC SYSTEM; CAUCASIAN; CONGENITAL DISORDER; FETUS; HEREDITY; HUMAN; NEWBORN; OXYGEN AFFINITY;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CHROMATOGRAPHY, DEAE-CELLULOSE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; FEMALE; FETAL HEMOGLOBIN; HEAT; HEMOGLOBINS, ABNORMAL; HUMAN; INFANT; MALE; OXYGEN; PEPTIDE FRAGMENTS; SUPPORT, U.S. GOV'T, P.H.S.; TRYPSIN;

EID: 0021218705     PISSN: 01674838     EISSN: None     Source Type: Journal    
DOI: 10.1016/0167-4838(84)90208-5     Document Type: Article

References (18)