檢索結果 - Cécile Méjécase

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  1. 1
    Practical guide to genetic screening for inherited eye diseases

    Practical guide to genetic screening for inherited eye diseases 由 Cécile Méjécase, Samantha Malka, Zeyu Guan, Amy Slater, Gavin Arno, Mariya Moosajee

    出版 2020
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    <i>MERTK</i> mutation update in inherited retinal diseases

    <i>MERTK</i> mutation update in inherited retinal diseases 由 Isabelle Audo, Saddek Mohand‐Saïd, Élise Boulanger-Scemama, Xavier Zanlonghi, Christel Condroyer, Vanessa Démontant, Fiona Boyard, Aline Antonio, Cécile Méjécase, Saïd El Shamieh, José‐Alain Sahel, Christina Zeitz

    出版 2018
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    Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to<i>CLN3</i>Pathogenic Variants in a French Retinitis Pigmentosa Cohort

    Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to<i>CLN3</i>Pathogenic Variants in a French Retinitis Pigmentosa Cohort 由 Vasily Smirnov, Marco Nassisi, Cyntia Solis Hernandez, Cécile Méjécase, Saïd El Shamieh, Christel Condroyer, Aline Antonio, Isabelle Meunier, Camille Andrieu, Sabine Defoort‐Dhellemmes, Saddek Mohand‐Saïd, José‐Alain Sahel, Isabelle Audo, Christina Zeitz

    出版 2021
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    Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy

    Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy 由 Christina Zeitz, Julien Navarro, Leila Azizzadeh Pormehr, Cécile Méjécase, Luiza M. Neves, Camille Letellier, Christel Condroyer, Shahad Albadri, Andréa Amprou, Aline Antonio, Tasnim Ben Yacoub, Juliette Wohlschlegel, Camille Andrieu, Malo Serafini, Lorenzo Bianco, Alessio Antropoli, Marco Nassisi, Saïd El Shamieh, Sandra Chantot‐Bastaraud, Saddek Mohand‐Saïd, Vasily Smirnov, José‐Alain Sahel, Filippo Del Bene, Isabelle Audo

    出版 2024
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