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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.
Zeitz, Christina; Méjécase, Cécile; Michiels, Christelle; Condroyer, Christel; Wohlschlegel, Juliette; Foussard, Marine; Antonio, Aline; Démontant, Vanessa; Emmenegger, Lisa; Schalk, Audrey; Neuillé, Marion; Orhan, Elise; Augustin, Sébastien; Bonnet, Crystel; Estivalet, Amrit; Blond, Frédéric; Blanchard, Steven; Andrieu, Camille; Chantot-Bastaraud, Sandra; Léveillard, Thierry; Mohand-Saïd, Saddek; Sahel, José-Alain; Audo, Isabelle.
Afiliação
  • Zeitz C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Méjécase C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Michiels C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Condroyer C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Wohlschlegel J; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Foussard M; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Antonio A; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Démontant V; CHNO des Quinze-Vingts, INSERM-DHOS CIC 1423, 75012 Paris, France.
  • Emmenegger L; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Schalk A; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Neuillé M; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Orhan E; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Augustin S; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Bonnet C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Estivalet A; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Blond F; Unité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75015 Paris, France.
  • Blanchard S; INSERM, Institut de l'Audition, Institut Pasteur, 75012 Paris, France.
  • Andrieu C; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Chantot-Bastaraud S; Unité de Génétique et Physiologie de l'Audition, Institut Pasteur, 75015 Paris, France.
  • Léveillard T; INSERM, Institut de l'Audition, Institut Pasteur, 75012 Paris, France.
  • Mohand-Saïd S; Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
  • Sahel JA; IntegraGen SA, Genopole, Campus, 91000 Evry, France.
  • Audo I; CHNO des Quinze-Vingts, INSERM-DHOS CIC 1423, 75012 Paris, France.
Int J Mol Sci ; 22(15)2021 Jul 23.
Article em En | MEDLINE | ID: mdl-34360642
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Potássio / Proteínas Mitocondriais / Distrofias de Cones e Bastonetes / Genes Recessivos / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Potássio / Proteínas Mitocondriais / Distrofias de Cones e Bastonetes / Genes Recessivos / Mutação Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França