APA

Shimozawa N., Nagase T., Takemoto Y., Suzuki Y. & Kondo N. (20040702). Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. : Advances in experimental medicine and biology.

Chicago

Shimozawa Nobuyuki, Nagase Tomoko, Takemoto Yasuhiko, Suzuki Yasuyuki and Kondo Naomi. 20040702. Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. : Advances in experimental medicine and biology.

Harvard

Shimozawa N., Nagase T., Takemoto Y., Suzuki Y. and Kondo N. (20040702). Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. : Advances in experimental medicine and biology.

MLA

Shimozawa Nobuyuki, Nagase Tomoko, Takemoto Yasuhiko, Suzuki Yasuyuki and Kondo Naomi. Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. : Advances in experimental medicine and biology. 20040702.