Fig. 3 | European Journal of Human Genetics

Fig. 3

From: Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy

Fig. 3The alternative text for this image may have been generated using AI.

Sanger sequencing of variants identified in CNTNAP1 in the affected brothers (patients 2 and 3) and their parents. Open symbols: unaffected; filled symbols: affected; square symbols: male and circular symbols: female The nucleotide and amino acid changes are indicated

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