Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation (Q24532123)

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Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
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    Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation (English)
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    Naomi Matsumoto
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    Shigehiko Tamura
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    Satomi Furuki
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    Non Miyata
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    Ann Moser
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    Nobuyuki Shimozawa
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    Hugo W Moser
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    Yasuyuki Suzuki
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    Naomi Kondo
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    Yukio Fujiki
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    August 2003
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    73
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    233-46
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    2
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