Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G→A mutation

Blood Cells, Molecules, and Diseases

Volumn 35, Issue 2, 2005, Pages 193-195

  Sukumar, Sridevi ^a   Mukherjee, Malay B ^a   Colah, Roshan B ^a   Mohanty, Dipika ^a  

^a KEM HOSPITAL   (India)

Author keywords

G6PD variants; India; Kerala Kalyan; Mutation

Indexed keywords

ADOLESCENT; ADULT; ANAMNESIS; ARTICLE; CASE REPORT; DNA DETERMINATION; DNA SEQUENCE; ELECTROPHORETIC MOBILITY; ENZYME DEFICIENCY; GENE MUTATION; GENETIC VARIABILITY; HEMOLYSIS; HUMAN; INDIA; MALE; MOLECULAR BIOLOGY; OUTPATIENT DEPARTMENT; PRIORITY JOURNAL;

ADOLESCENT; ANEMIA, HEMOLYTIC; ELECTROPHORESIS; ENZYME STABILITY; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; HYDROGEN-ION CONCENTRATION; INDIA; KINETICS; MALE; MIDDLE AGED; POINT MUTATION; VARIATION (GENETICS);

EID: 24644468992     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2005.03.001     Document Type: Article

References (11)

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