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Author Report for: Tazir M

No contact information in database for Tazir M

    Title: Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families
    Kediha MI, Tazir M, Magnouche C, Sternberg D, Belarbi S, Eymard B, Ali Pacha L
    Ref: Rev Neurol (Paris), :, 2023 : PubMed


    Title: Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism
    Fiskerstrand T, H'Mida-Ben Brahim D, Johansson S, M'Zahem A, Haukanes BI, Drouot N, Zimmermann J, Cole AJ, Vedeler C and Knappskog PM <9 more author(s)>
    Ref: American Journal of Human Genetics, 87:410, 2010 : PubMed


    Title: The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
    Richard P, Gaudon K, Haddad H, Ammar AB, Genin E, Bauche S, Paturneau-Jouas M, Muller JS, Lochmuller H and Hantai D <13 more author(s)>
    Ref: Neurology, 71:1967, 2008 : PubMed


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Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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