Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. In : Roels F, Baes M, De Bie S eds. Peroxisomal Disorders and Regulation of Genes
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. In : Roels F, Baes M, De Bie S eds. Peroxisomal Disorders and Regulation of Genes
复制标题
日本过氧化物酶体生物发生障碍患者的遗传异质性以及 PEX10 基因最常见突变的创始人单倍型的证据。
DOI：
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发表时间：
2003
期刊：
影响因子：
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通讯作者：
Kondo N.
中科院分区：
文献类型：
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作者：
Shimozawa N;Nagase T;Takemoto Y;Suzuki Y;Kondo N.
