Molecular and Genetic Studies of Congenital Myopathies
Conditions
Central Core Disease · Centronuclear Myopathy · Congenital Fiber Type Disproportion · Multiminicore Disease · Myotubular Myopathy · Nemaline Myopathy · Rigid Spine Muscular Dystrophy · Undefined Congenital Myopathy
Simple summaryAI-assisted
This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.
Locations
Genetics Division, Boston Children's Hospital, Boston, Massachusetts, United States
Contact: Study coordinator (Casie Genetti, M.S. C.G.C.) · BeggsLabGC@childrens.harvard.edu · (617) 919-2169Contact: Principal Investigator (Alan H. Beggs, Ph.D.)
Study leads
Alan H. Beggs, Ph.D.
Principal Investigator
Children's Hospital Boston/Harvard Medical School