Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

Reference

Meira, Lisiane B., et al. “Manitoba Aboriginal Kindred With Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene”. The American Journal of Human Genetics, vol. 66, no. 4, Mar. 2000, pp. 1221–1228, https://doi.org/10.1086/302867.

PubMed Reference Number (PMID)

10739753