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1دورية أكاديمية
المصدر: Cells, Vol 11, Iss 8, p 1373 (2022)
مصطلحات موضوعية: retina, zebrafish, cryoinjury, regeneration, Cytology, QH573-671
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Anaïs F. Poncet, Olivier Grunewald, Veronika Vaclavik, Isabelle Meunier, Isabelle Drumare, Valérie Pelletier, Béatrice Bocquet, Margarita G. Todorova, Anne-Gaëlle Le Moing, Aurore Devos, Daniel F. Schorderet, Florence Jobic, Sabine Defoort-Dhellemmes, Hélène Dollfus, Vasily M. Smirnov, Claire-Marie Dhaenens
المصدر: International Journal of Molecular Sciences, Vol 23, Iss 8, p 4294 (2022)
مصطلحات موضوعية: MFSD8 gene, isolated macular dystrophy, neuronal ceroid lipofuscinosis, deep intronic variant, transcript analysis, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
العلاقة: https://www.mdpi.com/1422-0067/23/8/4294Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test
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3دورية أكاديمية
المصدر: Cells, Vol 11, Iss 7, p 1088 (2022)
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
المصدر: Genes, Vol 11, Iss 5, p 503 (2020)
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
المصدر: Genes, Vol 10, Iss 12, p 953 (2019)
مصطلحات موضوعية: best1, bestrophinopathy, arb, Genetics, QH426-470
وصف الملف: electronic resource
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6
المؤلفون: Daniel F. Schorderet, Maria Helfenstein, Imen Habibi, Veronika Vaclavik, Ahmed Turki, Leila El Matri, Khaled El Matri, Stefan Wyrsch, Yosra Falfoul, Margarita G. Todorova
المصدر: Genes, Vol 11, Iss 503, p 503 (2020)
مصطلحات موضوعية: Genetics, lcsh:Genetics, n/a, lcsh:QH426-470, Biology, Gene, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Genetics (clinical), Autosomal recessive bestrophinopathy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fcd51551868300b9dd317b64e3f265aTest
https://www.mdpi.com/2073-4425/11/5/503Test -
7
المؤلفون: Ahmed Turki, Yosra Falfoul, Stefan Wyrsch, Maria Helfenstein, Margarita G. Todorova, Daniel F. Schorderet, Imen Habibi, Veronika Vaclavik, Khaled El Matri, Leila El Matri
المصدر: Genes, Vol 10, Iss 12, p 953 (2019)
Genes
Volume 10
Issue 12مصطلحات موضوعية: 0301 basic medicine, Male, Visual acuity, genetic structures, Eye, EOG light rise, 0302 clinical medicine, BEST1, Medicine, Bestrophins, Child, Genetics (clinical), Bestrophinopathy, Eye Diseases, Hereditary, Phenotype, Molecular analysis, Pedigree, best1, medicine.anatomical_structure, Female, medicine.symptom, Autosomal recessive bestrophinopathy, Optic disc, Adult, medicine.medical_specialty, Adolescent, lcsh:QH426-470, phenotype, Retinitis, arb, Article, 03 medical and health sciences, Young Adult, bestrophinopathy, Retinal Diseases, vitelliform macular dystrophy, Ophthalmology, Genetics, Electroretinography, Humans, Genetic Association Studies, business.industry, Correction, mutations, medicine.disease, eye diseases, Electrooculography, lcsh:Genetics, best1 gene, 030104 developmental biology, Mutation, 030221 ophthalmology & optometry, sense organs, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e27f1955e3efda9a3059903c2e30ddaTest
https://www.mdpi.com/2073-4425/10/12/953Test