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Figure 1 | BMC Neurology

Figure 1

From: Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Figure 1

Pedigrees of the 22 BFIE families and 8 ICCA families. The arrow indicates the proband. An individual with a heterozygous PRRT2 mutation is indicated by m/+, and an individual without a PRRT2 mutation is indicated by +/+. An individual with an asterisk is a patient with migraine. (A) Pedigrees of families 1-13: thirteen BFIE families with a PRRT2 mutation, (B) Pedigrees of families 14-22: nine BFIE families without a PRRT2 mutation, (C) Pedigrees of families 23-30: eight ICCA families with a PRRT2 mutation.

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BMC Neurology

ISSN: 1471-2377

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