Screening for the β-39 mutation in thalassemia by capillary electrophoresis in free solution in strongly acidic, isoelectric buffers

Electrophoresis

Volumn 21, Issue 4, 2000, Pages 780-784

  Gelfi, Cecilia ^a   Viganó, Agnese ^a   Carta, Piera ^b   Manchia, Pierangela ^b   Cossu, Gian Franco ^c   Righetti, Pier Giorgio ^d  

^a INSTITUTE OF BIOMEDICAL TECHNOLOGIES   (Italy)

^b Service of Immunohematology   (Italy)

^c Servizio di Igiene Pubblica   (Italy)

^d UNIVERSITY OF VERONA   (Italy)

Author keywords

Capillary electrophoresis; Point mutations; Thalassemia

Indexed keywords

AMINO ACIDS; DIAGNOSIS; HEMOGLOBIN; INDIUM COMPOUNDS;

ACIDIC BUFFERS; CHARGE DIFFERENCE; FAN OUT; FREE SOLUTIONS; GENOMIC DNA; ISOELECTRIC; NOVEL METHODS; POINT MUTATIONS; THALASSAEMIA; TITRATION CURVES;

CAPILLARY ELECTROPHORESIS;

BETA GLOBIN; DNA;

CAPILLARY ELECTROPHORESIS; CONFERENCE PAPER; GENE AMPLIFICATION; HUMAN; MISSENSE MUTATION; PH; POINT MUTATION; THALASSEMIA;

EID: 0034020424     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1522-2683(20000301)21:4<780::AID-ELPS780>3.0.CO;2-Y     Document Type: Conference Paper

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