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Fig. 3 | BMC Neurology

Fig. 3

From: Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review

Fig. 3

Schematic illustration of (A) wild-type TECPR2 and (B) Mutant TECPR2 with c.1568del; p.Ser523PhefsTer12, resulting in a frameshift and a premature stop codon. Tryptophan-aspartate (WD) repeats, the poly-lysine tract (polyK), and TECPR domains are significant conserved domains in the structure of the wild-type TECPR2

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BMC Neurology

ISSN: 1471-2377

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