A new Gγ chain variant: Hb F-Bron [γ20(B2) Val→Ala]

Hemoglobin

Volumn 29, Issue 4, 2005, Pages 301-305

  Lacan, Philippe ^a   Burnichon, Nelly ^a   Becchi, Michel ^b   Zanella Cleon, Isabelle ^b   Aubry, Martine ^a   Couprie, Nicole ^c   Francina, Alain ^a  

^a EDOUARD HERRIOT HOSPITAL   (France)

^b INSTITUT DE BIOLOGIE ET CHIMIE DES PROTÉINES   (France)

^c LMM Laboratoire Marcel Merieux   (France)

Author keywords

G gene; Fetal hemoglobin (Hb); Mass spectrometry (MS); Variant

Indexed keywords

GAMMA GLOBIN; HEMOGLOBIN CHAIN; HEMOGLOBIN F BRON; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

ALPHA THALASSEMIA; ARTICLE; DNA SEQUENCE; GENE DELETION; GENE INTERACTION; GENE STRUCTURE; GENETIC VARIABILITY; GLOBIN GENE; HEMATOLOGIC DISEASE; HETEROZYGOSITY; HUMAN; INFANT; IRON DEFICIENCY ANEMIA; MALE; MASS SPECTROMETRY; MICROCYTOSIS;

ALPHA-THALASSEMIA; ANEMIA, HYPOCHROMIC; DNA MUTATIONAL ANALYSIS; FETAL HEMOGLOBIN; GLOBINS; HEMOGLOBINS, ABNORMAL; HUMANS; INFANT, NEWBORN; MALE; MUTATION, MISSENSE; VARIATION (GENETICS);

EID: 28844498697     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260500312725     Document Type: Article

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