Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene

Shimozawa, N., Nagase, T., Takemoto, Y., Suzuki, Y., & Kondo, N. (2003). Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. In Advances in Experimental Medicine and Biology (Vol. 544, p. 71). Kluwer Academic/Plenum Publishers. https://doi.org/10.1007/978-1-4419-9072-3_10