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. Author manuscript; available in PMC: 2010 Jan 14.
Published in final edited form as: Neurobiol Aging. 2007 Jun 22;30(1):1–13. doi: 10.1016/j.neurobiolaging.2007.05.010

Fig. 2.

Fig. 2

FTDP-17 mutations and their location along human MAPT. Only the exons in which mutations have been reported are shown. Point mutations are indicated by the identity and site of the amino acid change. Splice site mutations in intron 10 are indicated by their position counting away from exon 10.