Skip to main content
. Author manuscript; available in PMC: 2012 Sep 6.
Published in final edited form as: Neuroreport. 2008 May 7;19(7):739–743. doi: 10.1097/WNR.0b013e3282fd6e88

Fig. 2.

Fig. 2

Sites of spontaneous mutation in mouse and human MAO A, exon 8. Arrows indicate sites of mutation resulting in premature stop codons in mouse (top) corresponding to amino acid 284 (lysine) and in human (bottom) corresponding to amino acid 296 (glutamine). Nucleic acid numbering is according to mouse MAO A GenBank entry NM_173740 and human gene bank entry M68840.