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Shimozawa Nobuyuki
Shimozawa Nobuyuki
Genetics
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Peroxin
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神経発達症群/神経発達障害群 遺伝的要因による神経発達障害 遺伝性代謝病 ペルオキシソーム病
2017
Shimozawa Nobuyuki
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AB067. X-linked adrenoleukodystrophy: Phenotype and genotype in Vietnamese patients
2017
Annals of Translational Medicine
Khanh Ngoc Nguyen
Ha Thu Nguyen
Ngoc Thi Bich Can
Thao Phuong Bui
Shimozawa Nobuyuki
Huynh Anh Vu
Mai Thi Thanh Do
Dung Chi Vu
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相補グループ8のペルオキシソーム生物発生疾患を起因する新しいperoxin遺伝子PEX26における変異は遺伝子型-表現型相互関連を供する(Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation)
2003
Furuki Satomi
Tamura Shigehiko
Matsumoto Naomi
Miyata Non
Moser Ann
Shimozawa Nobuyuki
W Moser Hugo
Suzuki Yasuyuki
Kondo Naomi
Fujiki Yukio
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相補グループ8のペルオキシソーム生物発生疾患を起因する新しいperoxin遺伝子PEX26における変異は遺伝子型-表現型相互関連を供する(Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation)
2003
Furuki Satomi
Tamura Shigehiko
Matsumoto Naomi
Miyata Non
Moser Ann
Shimozawa Nobuyuki
W Moser Hugo
Suzuki Yasuyuki
Kondo Naomi
Fujiki Yukio
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