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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1

Fig. 3

Mutations identified in the probands of Families 1–11. Mutations detected by Sanger sequencing: a: Patient 1, c.1246C>T; b: Patient 4, c.4802delT; c: Patient 7, c.5428delT; d: Patient 11, c.3826C>T; e: Patient 13, c.5791T>C; f: Patient 15, c.2062G>T; g: Patient 16, c.4469T>C; h: Patient 17 c.1885G>A; i: Patient 18, c.1754_1757delTAAC; j: Patient 19, c.6102C>A; k: Patient 20, c.6791dupA

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