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. 2002 Apr;55(2):127–144. doi: 10.1136/mp.55.2.127

Figure 10.

Figure 10

Arginine residues encoded by CGA within (A) the factor VIII and (B) the factor IX protein sequences. Nonsense mutations are brought about by C to T transition within the CG site of these codons. These are recurrent gene defects within haemophilia populations.