Works matching AU Monica Robertella

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.

Published in:

Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 452, doi. 10.1093/brain/awn325

By:

• Joachim Schessl;
• Ana L. Taratuto;
• Caroline Sewry;
• Roberta Battini;
• Steven S. Chin;
• Baijayanta Maiti;
• Alberto L. Dubrovsky;
• Marcela G. Erro;
• Graciela Espada;
• Monica Robertella;
• Maria Saccoliti;
• Patricia Olmos;
• Leslie R. Bridges;
• Peter Standring;
• Ying Hu;
• Yaqun Zou;
• Kathryn J. Swoboda;
• Mena Scavina;
• Hans-Hilmar Goebel;
• Christina A. Mitchell

Publication type:

Article