Familial hypomagnesemia with hypercalciuria and nephrocalcinosis : unusual clinical associations and novel claudin16 mutation in an Egyptian family
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概要
- 論文の詳細を見る
- 2009-08-01
著者
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Tajima Toshihiro
Department of Pediatrics, Hokkaido University, School of Medicine
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Fujieda Kenji
Department of Pediatrics, Asahikawa Medical College
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Darwish Ahmad
Nephrology Unit Mansoura University Children's Hospital
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Fujieda Kenji
Department Of Pediatrics Asahikawa Medical College
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Tajima Toshihiro
Department Of Pediatrics Hokkaido University School Of Medicine
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AL-HAGGAR Mohammad
Genetics Unit, Mansoura University Children's Hospital
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BAKR Ashraf
Nephrology Unit, Mansoura University Children's Hospital
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HAMMAD Ayman
Nephrology Unit, Mansoura University Children's Hospital
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SOLIMAN Othman
Genetics Unit, Mansoura University Children's Hospital
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AL-SAID Afaf
Genetics Unit, Mansoura University Children's Hospital
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YAHIA Sohier
Genetics Unit, Mansoura University Children's Hospital
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ABDEL-HADY Dina
Genetics Unit, Mansoura University Children's Hospital
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Bakr Ashraf
Nephrology Unit Mansoura University Children's Hospital
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Yahia Sohier
Genetics Unit Mansoura University Children's Hospital
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Al-said Afaf
Genetics Unit Mansoura University Children's Hospital
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Hammad Ayman
Nephrology Unit Mansoura University Children's Hospital
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Soliman Othman
Genetics Unit Mansoura University Children's Hospital
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Al-haggar Mohammad
Genetics Unit Mansoura University Children's Hospital
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Abdel-hady Dina
Genetics Unit Mansoura University Children's Hospital
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Tajima Toshihiro
Department Of Pediatrics Hokkaido University Graduate School Of Medicine
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