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
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概要
- 論文の詳細を見る
- 2012-03-01
著者
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Saad Ali
Laboratoire De Cytogenetique De Genetique Moleculaire Et De Biologie De La Reproduction Humaines Hop
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Mamay Ons
Laboratoire De Cytogenetique De Genetique Moleculaire Et De Biologie De La Reproduction Humaines Hop
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Gribaa Moez
Laboratoire De Cytogenetique De Genetique Moleculaire Et De Biologie De La Reproduction Humaines Hop
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Adala Labiba
Laboratoire De Cytogenetique De Genetique Moleculaire Et De Biologie De La Reproduction Humaines Hop
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MILI Amira
Laboratory of Human Cytogenetic, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital
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CHARFEDDINE Ilhem
Laboratory of Human Cytogenetic, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital
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MAMAI Ons
Laboratory of Human Cytogenetic, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital
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CHERIF Wafa
Molecular Investigation of Genetic Orphan Diseases Research Unit UR04/SP03, Pasteur Institute
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AMARA Abdelbasset
Laboratory of Human Cytogenetic, Molecular Genetics and Biology of Reproduction, Farhat Hached University Hospital
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PAGLIARANI Serena
Dino Ferrari Center, Department of Neurological Sciences, University of Milan, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangialli e Regina Elena
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LUCCHIARI Sabrina
Dino Ferrari Center, Department of Neurological Sciences, University of Milan, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangialli e Regina Elena
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AYADI Abdelkarim
Paediatric Department, Tahar Sfar University Hospital
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TEBIB Neji
Paediatric Department, La Rabta University Hospital
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HARBI Abdelaziz
Paediatric Department, Sahloul University Hospital
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BOUGUILA Jihene
Paediatric Department, Farhat HACHED University Hospital
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LIMEM Khalifa
Department of Biochemistry, Faculty of Medicine, University of Sousse
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COMI GP
Dino Ferrari Center, Department of Neurological Sciences, University of Milan, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangialli e Regina Elena
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Comi Gp
Dino Ferrari Center Department Of Neurological Sciences University Of Milan Fondazione Irccs Ospedale Maggiore Policlinico Mangialli E Regina Elena
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Tebib Neji
Paediatric Department La Rabta University Hospital
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Cherif Wafa
Molecular Investigation Of Genetic Orphan Diseases Research Unit Ur04/sp03 Pasteur Institute
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Limem Khalifa
Department Of Biochemistry Faculty Of Medicine University Of Sousse
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Harbi Abdelaziz
Paediatric Department Sahloul University Hospital
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Bouguila Jihene
Paediatric Department Farhat Hached University Hospital
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Charfeddine Ilhem
Laboratory Of Human Cytogenetic Molecular Genetics And Biology Of Reproduction Farhat Hached University Hospital
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Pagliarani Serena
Dino Ferrari Center Department Of Neurological Sciences University Of Milan Fondazione Irccs Ospedale Maggiore Policlinico Mangialli E Regina Elena
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Lucchiari Sabrina
Dino Ferrari Center Department Of Neurological Sciences University Of Milan Fondazione Irccs Ospedale Maggiore Policlinico Mangialli E Regina Elena
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Amara Abdelbasset
Laboratory Of Human Cytogenetic Molecular Genetics And Biology Of Reproduction Farhat Hached University Hospital
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Ayadi Abdelkarim
Paediatric Department Tahar Sfar University Hospital
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Mili Amira
Laboratory Of Human Cytogenetic Molecular Genetics And Biology Of Reproduction Farhat Hached University Hospital
関連論文
- Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations
- An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation
- Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type ？
- 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