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Questions related from Samer Ismail
We sequence patients DNA in order to detect the different mutations associated with the disorders; if it is simple gene with few exons and small number of patients then it is feasible to use...
25 December 2014 8,887 10 View
We usually explain mutation effects based on the amino acid codon (silent, mis-sense, non-sense) if it takes place in an exon, but what is the situation if it takes place in an intron or in...
10 December 2014 9,780 12 View