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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants

Fig. 2

Sanger traces for PCR products of the patient and his parents. a Sanger traces for PCR products of the patient showed the two heterozygous null variants in CLN8 (c.298C > T, p.Gln100Ter; c.551G > A, p.Trp184Ter). b Sanger traces for PCR products of his father, which confirmed that the c.298 C > T variant was inherited from the father. c Sanger traces for PCR products of his mother, which confirmed that the c.551 G > A variant was inherited from the mother

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BMC Medical Genetics

ISSN: 1471-2350

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