A novel mutation in licam gene in a japanese patient with X-linked hydrocephalus

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Abstract

L1CAM is a member of the immunoglobulin gene superfamily of neural adhesion molecule. Abnormality of the L1CAM gene is associated with X-linked recessive form of congenital hydrocephalus (HSAS; hydrocephalus due to congenital stenosis of aqueduct of Sylvius) and some allelic disorders. Four new patients with congenital hydrocephalus consistent with the X-linked type were described. One of them had a novel mutation in the L1CAM gene.

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Okamoto, N., Wada, Y., Kawabata, H., Ishikiriyama, S., & Takahashi, S. (1996). A novel mutation in licam gene in a japanese patient with X-linked hydrocephalus. Journal of Human Genetics, 41(4), 431–437. https://doi.org/10.1007/bf01876336

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