Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family : exclusion of the PRPH2 gene and the 17p13 locus
スポンサーリンク
概要
- 論文の詳細を見る
- 2009-10-01
著者
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Rebai Ahmed
Department Of Bioinformatics Center Of Biotechnology Of Sfax
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Chakroun Sonia
Research Unit Of Molecular Investigation Of Genetic Orphan Diseases Ur04sp03 Pasteur Institute
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OUECHTATI Farah
Molecular Investigation of Genetic Orphan Diseases Research Unit UR04/SP03, Pasteur Institute
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Ouechtati Farah
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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Tahar Olfa
Department Of Ophthalmology La Rabta Hospital
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MHENNI Amin
Department of Ophthalmology, La Rabta Hospital
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CHAKROUN Sonia
Oculogenetics Unit, Hedi Rais Institute of Ophthalmology of Tunis
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CHOUCHENE Ibtissem
Molecular Investigation of Genetic Orphan Diseases, Pasteur Institute
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OUESLATI Souad
U05/UR08-02 Inherited Neurological Child Diseases, Faculty of Medicine of Tunis
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REBAI Ahmed
Unit of Bioinformatics, Center of Biotechnology
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ABDELHAK Sonia
Oculogenetics Unit, Hedi Rais Institute of Ophthalmology of Tunis
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JEDDI-BLOUZA Amel
Department of Ophthalmology, La Rabta Hospital
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Mhenni Amin
Department Of Ophthalmology La Rabta Hospital
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Oueslati Souad
U05/ur08-02 Inherited Neurological Child Diseases Faculty Of Medicine Of Tunis
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Jeddi-blouza Amel
Department Of Ophthalmology La Rabta Hospital
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Chouchene Ibtissem
Molecular Investigation Of Genetic Orphan Diseases Pasteur Institute
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Abdelhak Sonia
Research Unit Of Molecular Investigation Of Genetic Orphan Diseases Ur04sp03 Pasteur Institute
関連論文
- Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region
- Genetic heterogeneity of megaloblastic anaemia type 1 in Tunisian patients
- Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations
- Clinical and genetic investigation of a large Tunisian family with complete achromatopsia : identification of a new nonsense mutation in GNAT2 gene
- Central areolar choroidal dystrophy associated with inherited drusen in a multigeneration Tunisian family : exclusion of the PRPH2 gene and the 17p13 locus
- Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian family