Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy
The American Journal of Human Genetics2007Vol. 81(5), pp. 884–894
Citations Over TimeTop 10% of 2007 papers
Richard J.L.F. Lemmers, Mariëlle Wohlgemuth, Kristiaan J. van der Gaag, Patrick J. van der Vliet, Corrie M.M. van Teijlingen, Peter de Knijff, George W. Padberg, Rune R. Frants, Silvère M. van der Maarel
Related Papers
- → Three novel serum biomarkers, miR-1, miR-133a, and miR-206 for Limb-girdle muscular dystrophy, Facioscapulohumeral muscular dystrophy, and Becker muscular dystrophy(2014)101 cited
- → Serum miRNAs as biomarkers for the rare types of muscular dystrophy(2022)15 cited
- → The muscular dystrophies and related disorders. II. Diseases simulating muscular dystrophies(1978)1 cited
- Susquehanna Chorale Spring Concert "Roots and Wings"(2017)
- → DETERMINING QUALITY REQUIREMENTS AT THE UNIVERSITIES TO IMPROVE THE QUALITY OF EDUCATION(2018)