Journal article

Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies

Minttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, Tuula A Nyman, Christine Barnerias, Alan H Beggs, Enrico Bertini, Oezge Ceyhan-Birsoy, Pascal Cintas, Marion Gerard, Brigitte Gilbert-Dussardier, Jacob S Hogue, Cheryl Longman, Bruno Eymard, Moshe Frydman, Peter B Kang, Lars Klinge, Hanna Kolski, Hans Lochmueller, Laurent Magy Show all

Human Mutation | WILEY-BLACKWELL | Published : 2014

Grants

Awarded by National Institute of Arthritis and Musculoskeletal and Skin Diseases of the NIH


Awarded by Muscular Dystrophy Association


Awarded by Australian National Health, Medical Research Council (NHMRC)


Awarded by NHMRC Centre of Research Excellence


Awarded by NHMRC of Australia


Awarded by Telethon


Awarded by European Union


Awarded by British Heart Foundation


Awarded by Medical Research Council


Funding Acknowledgements

Contract grant sponsors: National Institute of Arthritis and Musculoskeletal and Skin Diseases of the NIH (grant R01 AR044345); Muscular Dystrophy Association (MDA201302); Australian National Health, Medical Research Council (NHMRC) Project (grant APP1022707); NHMRC Centre of Research Excellence (grant APP1031893); NHMRC of Australia (APP1035828, APP1026933); Telethon GUP08005; European Union Seventh Framework Programme (FP7/2007-2013) (grant agreement no. 305444 (RD-Connect) and 305121 (Neuromics); Association Francaise contre les Myopathies; Sigrid Juselius Foundation; Academy of Finland; Finska Lakaresallskapet; Medicinska understodsforeningen Liv och Halsa r.f.; DHFMR; Foundation for Building Strength for Nemaline Myopathy; Ricerca Finalizzata Ministry of Health; British Heart Foundation.