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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Nat Genet. 2008 Dec 11;41(3):354–358. doi: 10.1038/ng.306

Figure 2.

Figure 2

A. Family used to identify region on chromosome 12 harbouring genetic defect causing nIHH with detail of subset of genes in critical interval B. Location of pathogenic mutation in TAC3. Shaded amino acids represent the tachykinin signature motif. C. Conservation of mutated residue among selected paralogues and orthologues.