A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach. (Q50595927)
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English | A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach. |
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A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach. (English)
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K Dörre
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M Olczak
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Y Wada
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P Sosicka
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M Grüneberg
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J Reunert
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G Kurlemann
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B Fiedler
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S Biskup
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K Hörtnagel
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S Rust
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T Marquardt
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17 March 2015
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38
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931-940
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5
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