Last Updated: 09/26/2026
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Found 3 publications
Illness-associated muscle weakness in dystroglycanopathies.
Journal: Neurology
Published: June 01, 2017
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.
Journal: Neuromuscular disorders : NMD
Published: September 28, 2013
Infantile onset CMT2D/dSMA V in monozygotic twins due to a mutation in the anticodon-binding domain of GARS.
Journal: Journal of the peripheral nervous system : JPNS
Published: April 03, 2012
Showing 1-3 of 3
Last Updated: 09/26/2026