genetics mutations and phenotype
can someone explain me why this result is observed in f1 generation here where crossing them can result in complete deactivation of B mutant
A and B are two recessive mutants. C is a protein product of a gene
A- defective in activation of B and defective in C activation B- defective in C activation
F1 generation the cross between A and B >
Ax B : F1 progeny defective in c activation
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Hi There, could you please explain how this is related to bioinformatics and what is the specific bioinformatics problem being tackled?
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