Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in<i>TPM2</i>and<i>TPM3</i>Causing Congenital Myopathies
M. Marttila(Boston Children's Hospital), Carina Wallgren‐Pettersson(University of Helsinki), Ekkehard Wilichowski(University of Göttingen), Ozge Ceyhan‐Birsoy(Memorial Sloan Kettering Cancer Center), Jacob S. Hogue(University of California, San Francisco), Kathryn N. North(Children's Hospital at Westmead), Kristen L. Nowak(The University of Western Australia), Vilma‐Lotta Lehtokari(University of Helsinki), Frank J. Probst(Baylor College of Medicine), Sylviane Peudenier-Robert(Centre Hospitalier Régional Universitaire de Brest), William Stewart(New Jersey Institute of Technology), Nigel G. Laing(Harry Perkins Institute of Medical Research), Cheryl Longman, Hanna Kolski(University of Alberta), Brigitte Gilbert‐Dussardier(Laboratoire de Génétique Cellulaire), Eugenio Mercuri(Università Cattolica del Sacro Cuore), Marion Gérard(Hôpital Georges-Clemenceau), Helena Pihko(Helsinki University Hospital), Mikaela Grönholm(University of Helsinki), Moshe Frydman(Tel Aviv University), Alan H. Beggs(Broad Institute), B. Eymard(University Hospital of Basel), Enrico Bertini(Bambino Gesù Children's Hospital), Peter B. Kang(Boston Children's Hospital), Hanns Lochmüller(Muscular Dystrophy UK), Christine Barnérias(Hôpital Necker-Enfants Malades), J. Winer(Queen Elizabeth Hospital Birmingham), Nicole Monnier(Inserm), Tuula A. Nyman(University of Helsinki), Nigel F. Clarke(Newcastle University), Laurent Magy(Hôpital Dupuytren), Katarina Pelin(University of Helsinki), Ricardo Reisin, Lars Klinge, Pascal Cintas(Université Fédérale de Toulouse Midi-Pyrénées), Steven B. Marston(Imperial College London), Véronique Manel(Hôpital Femme Mère Enfant), Tom Winder(University of Cambridge), Ana Lía Taratuto(Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia), M. Mayer(Sorbonne Université)
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