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Molecular Investigation of Genetic Orphan Diseases Research Unit UR04/SP03, Pasteur Institute | 論文
- Clinical and genetic investigation of a large Tunisian family with complete achromatopsia : identification of a new nonsense mutation in GNAT2 gene
- Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III : This article has been corrected since advance Online Publication, and a corrigendum is also printed in this issue
- 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