Hasil Pencarian - Vanita Berry

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  1. 1
    Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British family

    Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British f... oleh Michel Michaelides, Michalis Georgiou, Vanita Berry, Alexander Ionides, Roy A Quinlan

    Diterbitkan 2023-06-01
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  2. 2
    Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans

    Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans oleh Emilia Boiadjieva Knöpfel, Emilia Boiadjieva Knöpfel, Emilia Boiadjieva Knöpfel, Clara Vilches, Clara Vilches, Simone M. R. Camargo, Simone M. R. Camargo, Ekaitz Errasti-Murugarren, Ekaitz Errasti-Murugarren, Andrina Stäubli, Andrina Stäubli, Clara Mayayo, Clara Mayayo, Francis L. Munier, Nataliya Miroshnikova, Nadège Poncet, Nadège Poncet, Alexandra Junza, Alexandra Junza, Shomi S. Bhattacharya, Shomi S. Bhattacharya, Esther Prat, Esther Prat, Esther Prat, Vanita Berry, Wolfgang Berger, Wolfgang Berger, Wolfgang Berger, Elise Heon, Anthony T. Moore, Anthony T. Moore, Anthony T. Moore, Óscar Yanes, Óscar Yanes, Virginia Nunes, Virginia Nunes, Virginia Nunes, Manuel Palacín, Manuel Palacín, Manuel Palacín, Francois Verrey, Francois Verrey, Francois Verrey, Barbara Kloeckener-Gruissem, Barbara Kloeckener-Gruissem

    Diterbitkan 2019-06-01
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