Figure 1 | Human Genome Variation

Figure 1

From: A novel BBS10 mutation identified in a patient with Bardet–Biedl syndrome with a violent emotional outbreak

Figure 1

Sanger sequences of the patient and parents in BBS10 and predicted amino acid sequences. (a) The patient and mother have NM_024685.3:c.1677C>A mutation (arrow), which causes the termination of the BBS10 protein. (b) The patient and father have NM_024685.3:c.1974T>G mutation (arrow), which causes the termination of the protein. Thus, the patient has compound heterozygous mutations in the BBS10 gene.

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