Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients
スポンサーリンク
概要
著者
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Tasdemir Haydar
Department Of Child Neurology Faculty Of Medicine University Of Hacettepe
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Topaloglu Haluk
Department Of Child Neurology Faculty Of Medicine University Of Hacettepe
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DINCER Pervin
Department of Medical Biology, Faculty of Medicine, University of Hacettepe
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AYTER Sukruye
Department of Medical Biology, Faculty of Medicine, University of Hacettepe
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OZGUC Meral
Department of Medical Biology, Faculty of Medicine, University of Hacettepe
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RENDA Yavuz
Department of Child Neurology, Faculty of Medicine, University of Hacettepe
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Ozguc Meral
Department Of Medical Biology Faculty Of Medicine University Of Hacettepe
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Renda Yavuz
Department Of Child Neurology Faculty Of Medicine University Of Hacettepe
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Ayter Sukruye
Department Of Medical Biology Faculty Of Medicine University Of Hacettepe
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Dincer Pervin
Department Of Medical Biology Faculty Of Medicine University Of Hacettepe
関連論文
- Congenital muscular dystrophy with eye and brain involvement The Turkish experience in two cases
- Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients
- Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers
- Is oxidative damage in operation in patients with hereditary spastic paraparesis?
- Bone mineral density in children with cerebral palsy
- Deletion analysis in Turkish patients with spinal muscular atrophy
- Sandhoff disease in the Turkish population