Auteur

Khedhiri Souhir

Œuvres

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease

Documents

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease

Khedhiri Souhir, Chkioua Latifa, Ferchichi Salima, Miled Abdelhedi, Laradi, Laradi Sandrine

Documents

Savoirs

Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease

Khedhiri Souhir, Chkioua Latifa, Ferchichi Salima, Miled Abdelhedi, Laradi, Laradi Sandrine

5 pages

English

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Infos

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms

Documents

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms

Chkioua Latifa, Khedhiri Souhir, Kassab Asma, Bibi Amina, Ferchichi Salima, Froissart Roseline, Vianey-Saban Christine, Laradi Sandrine, Miled, Miled Abdelhedi

Documents

Savoirs

Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms

Chkioua Latifa, Khedhiri Souhir, Kassab Asma, Bibi Amina, Ferchichi Salima, Froissart Roseline, Vianey-Saban Christine, Laradi Sandrine, Miled, Miled Abdelhedi

8 pages

English

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Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population

Documents

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population

Chkioua Latifa, Khedhiri Souhir, Ben, Chahed Henda, Ferchichi Salima, Laradi Sandrine, Miled, Miled Abdelhedi

Documents

Savoirs

Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population

Chkioua Latifa, Khedhiri Souhir, Ben, Chahed Henda, Ferchichi Salima, Laradi Sandrine, Miled, Miled Abdelhedi

7 pages

English

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Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients

Documents

Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients

Chkioua Latifa, Khedhiri Souhir, Turkia Hadhami, Tcheng Rémy, Froissart Roseline, Chahed Henda, Ferchichi Salima, Ben, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi

Documents

Savoirs

Mucopolysaccharidosis type I: molecular characteristics of two novel alpha-L-iduronidase mutations in Tunisian patients

Chkioua Latifa, Khedhiri Souhir, Turkia Hadhami, Tcheng Rémy, Froissart Roseline, Chahed Henda, Ferchichi Salima, Ben, Vianey-Saban Christine, Laradi Sandrine, Miled Abdelhedi

6 pages

English

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