Fig. 4From: Novel detection of mutation in the TECPR2 gene in a Chinese hereditary spastic paraplegia 49 patient: a case reportMissense variants in the patient, his mother, and his father by WES. A variant c.1729C > T caused the amino acid change p.H577Y in TECPR2 and was inherited from the father. B variant c.4189G > A caused the amino acid change p.A1397T in TECPR2 and was inherited from the motherBack to article page