Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B

Kanji Okumoto, Ryota Itoh, Nobuyuki Shimozawa, Yasuyuki Suzuki, Shigehiko Tamura, Naomi Kondo, Yukio Fujiki

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90 Citations (Scopus)

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Medicine & Life Sciences