Abstract
C untilfurther use. Genomic DNA was extracted from whole bloodof the G6PD deficient subjects using DNA extraction kit(Roche Molecular Biochemicals, Switzerland). All sampleswere analysed by PCR-RFLP method for the G1003A muta-tion in exon 9 which is characteristic of G6PD Chatham. ForPCR reaction, the forward and reverse primers were: 5 -CAAGGA GCC CAT TCT CTC CCT T-3 and 5 -TTC TCC ACATAG AGG ACG ACG GCT GCC AAA GT-3 respectively(Rahimi
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
