Gagnon C

ORCID: 0000-0003-2829-8470 · 2 papers in corpus
review 2018
Neurology. Clinical practice ·doi:10.1212/cpj.0000000000000531

PURPOSE OF REVIEW: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No evidence-based guideline exists to inform the care of these patients, and most do…

review 1994
Advances in experimental medicine and biology ·doi:10.1007/978-1-4615-1833-4_14