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Volumn 26, Issue 2, 2002, Pages 181-184
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Hb Delfzicht [α9(A7)Asn→Lys (α1)]: A new, clinically silent hemoglobin variant observed in a Dutch patient
a a a b c a |
Author keywords
[No Author keywords available]
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Indexed keywords
HEMOGLOBIN;
HEMOGLOBIN DELFZICHT;
HEMOGLOBIN VARIANT;
AGED;
ALPHA GLOBIN GENE;
ALPHA THALASSEMIA;
ARTICLE;
BETA THALASSEMIA;
BLOOD SAMPLING;
CASE REPORT;
CHROMATOGRAPHY;
DIABETES MELLITUS;
ELECTROPHORESIS;
FEMALE;
GEL ELECTROPHORESIS;
GENE;
HEMOGLOBINOPATHY;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
PH;
POINT MUTATION;
PROTEIN VARIANT;
SICKLE CELL ANEMIA;
GENETIC VARIABILITY;
GENETICS;
HETEROZYGOTE;
ISOELECTRIC FOCUSING;
NETHERLANDS;
NUCLEOTIDE SEQUENCE;
PHENOTYPE;
AGED;
BASE SEQUENCE;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
FEMALE;
HEMOGLOBINS, ABNORMAL;
HETEROZYGOTE;
HUMANS;
ISOELECTRIC FOCUSING;
NETHERLANDS;
PHENOTYPE;
POINT MUTATION;
VARIATION (GENETICS);
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EID: 0036068486
PISSN: 03630269
EISSN: None
Source Type: Journal
DOI: 10.1081/HEM-120005457 Document Type: Article |
Times cited : (2)
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References (8)
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