Hb Campinas [α26(B7)Ala → Val]: A novel, electrophoretically silent, variant

Hemoglobin

Volumn 24, Issue 2, 2000, Pages 143-148

  Wenning, M R S C ^a   Silva, N M ^a   Jorge, S B ^a   Kimura, E M ^a   Costa, F F ^a   Torsoni, M A ^a   Ogo, S H ^a   Sonati, Maria De Fatima ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN VARIANT; GLOBIN; HEMOGLOBIN CAMPINAS;

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; ELECTROPHORESIS; GENE MUTATION; GENE SEQUENCE; HEMOGLOBINOPATHY; HUMAN; MALE; SCHOOL CHILD; ADULT; AMINO ACID SUBSTITUTION; BRAZIL; CAUCASIAN; CHEMISTRY; FAMILY HEALTH; FEMALE; GENETIC VARIABILITY; GENETICS; HETEROZYGOTE; MOTHER; NUCLEOTIDE SEQUENCE; POINT MUTATION;

ADULT; AMINO ACID SUBSTITUTION; BRAZIL; CHILD; DNA MUTATIONAL ANALYSIS; ELECTROPHORESIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; FAMILY HEALTH; FEMALE; GLOBINS; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HUMANS; MALE; MOTHERS; POINT MUTATION; VARIATION (GENETICS);

EID: 0033623698     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630260009003434     Document Type: Article

References (13)

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