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Fig. 2 | BMC Medical Genetics

Fig. 2

From: The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report

Fig. 2

Electropherograms for the family YUHL-165 showing the heterozygous R1890C and H1400Y mutations of TECTA in the proband and only the H1400Y mutation in the father. a Segregation of the TECTA gene showing the H1400Y substitution. b Segregation of the TECTA gene showing the R1890C substitution. c Use of synonymous variant in the TECTA gene for cis/trans status determination of the two missense variants

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