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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:
Zeitz, Christina
;
Méjécase, Cécile
;
Michiels, Christelle
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22157875. , 2021
Link:
https://inserm.hal.science/inserm-03841438
RT Journal T1
Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy
UL https://suche.suub.uni-bremen.de/peid=base-ftsorbonneuniv:oai:HAL:inserm-03841438v1&Exemplar=1&LAN=DE A1 Zeitz, Christina A1 Méjécase, Cécile A1 Michiels, Christelle A1 Condroyer, Christel A1 Wohlschlegel, Juliette A1 Foussard, Marine A1 Antonio, Aline A1 Démontant, Vanessa A1 Emmenegger, Lisa A1 Schalk, Audrey A1 Neuillé, Marion A1 Orhan, Elise A1 Augustin, Sébastien A1 Bonnet, Crystel A1 Estivalet, Amrit A1 Blond, Frédéric A1 Blanchard, Steven A1 Andrieu, Camille A1 Chantot-Bastaraud, Sandra A1 Léveillard, Thierry A1 Mohand-Saïd, Saddek A1 Sahel, José-Alain A1 Audo, Isabelle PB HAL CCSD; MDPI YR 2021 K1 CCDC51 K1 MITOK K1 candidate gene K1 inner segments K1 mitochondrial protein K1 retina K1 retinitis pigmentosa K1 rod-cone dystrophy K1 MESH: Adult K1 MESH: Cone-Rod Dystrophies K1 MESH: Humans K1 MESH: Male K1 MESH: Mitochondrial Proteins K1 MESH: Mutation K1 MESH: Pedigree K1 MESH: Phenotype K1 MESH: Potassium Channels K1 MESH: Female K1 MESH: Genes K1 Recessive K1 [SDV]Life Sciences [q-bio] K1 [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics JF info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms22157875 LK http://dx.doi.org/https://inserm.hal.science/inserm-03841438 DO https://inserm.hal.science/inserm-03841438 SF ELIB - SuUB Bremen
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