Fig. 2 | Journal of Human Genetics

Fig. 2

From: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease

Fig. 2

Four pedigrees affected by the c.1617del variant of TMEM260 and their sequence chromatograms. Participants with and without CHD are shown as filled and unfilled symbols, respectively. CHD congenital heart disease, NA not analyzed, PA-VSD pulmonary atresia with ventricular septal defect, PTA persistent truncus arteriosus, TOF Tetralogy of Fallot, VT variant type, WT wild-type

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