Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] associated with β0-thalassemia in a Sicilian child

Hemoglobin

Volumn 32, Issue 6, 2008, Pages 582-587

  Cuccia, Liana ^a,c   Saieva, Laura ^a   Borsellino, Zelia ^a   Marocco, Maria R ^a   Ruffo, Giovan B ^a   Riou, Jean ^b   Capra, Marcello ^a  

^a PO G di Cristina   (Italy)

^b HENRI MONDOR HOSPITAL   (France)

^c ARNAS Civico di Cristina Ascoli   (Italy)

Author keywords

Thalassemia ( thal); Hb Hinwil; Hemoglobins (Hbs) with high oxygen affinity

Indexed keywords

ASPARAGINE; HEMOGLOBIN VARIANT; THREONINE; HEMOGLOBIN HINWIL; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; BETA THALASSEMIA; CASE REPORT; CLINICAL FEATURE; CODON; CONTROLLED STUDY; ERYTHROCYTOSIS; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; INFANT; ISOELECTRIC FOCUSING; ITALY; MICROCYTOSIS; POLYACRYLAMIDE GEL ELECTROPHORESIS; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; THORAX RADIOGRAPHY; X RAY; ADULT; GENETICS; MALE; MUTATION; POLYCYTHEMIA;

BETA-THALASSEMIA; FEMALE; HEMOGLOBINS, ABNORMAL; HUMANS; INFANT; MALE; MUTATION; POLYCYTHEMIA; SICILY; YOUNG ADULT;

EID: 57449093200     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260802507766     Document Type: Article

References (5)

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