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Figure 3.

Sequence chromatograms from normal individual (wild type, WT) and affected individuals (P) are shown together with the expected amino-acid changes. Nucleotide variations are indicated by an arrow. A: 1364C>A inducing the A455D mutation in Patient 1 (P1), B: 1213G>T inducing the V405L mutation in Patient 7 (P7).

Neurogenetics. 2004 February; 5(1): 27–34.
Published online 2003 December 2. doi: 10.1007/s10048-003-0165-9.