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Aberrant Splicing of <i>DNM1L</i> Impairs Cardiac Bioenergetics and Mitochondrial Dynamics in Myotonic Dystrophy Type I (DM1). [PDF]

Circ Genom Precis Med
Adesanya O, Nabie P, Betancourt A, Kalsotra A.   +3 more
europepmc   +1 more source

Muscle-driven spinal cord histological and transcriptomic alterations in a myotonic dystrophy mouse model: insights into neuropathy. [PDF]

Brain Commun
Shi G, Luan Y, Ouyang Y, Chen K, Zhang K, Wen Z, Yang H, Huang K.   +7 more
europepmc   +1 more source

Multisystem Symptoms in Myotonic Dystrophy Type 1: A Management and Therapeutic Perspective. [PDF]

Int J Mol Sci
Kuntawala DH, Vitorino R, Cruz AC, Martins F, Rebelo S.   +4 more
europepmc   +1 more source

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Myotonic Dystrophy

Continuum, 2022
Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are genetic disorders affecting skeletal and smooth muscle, heart, brain, eyes, and other organs. The multisystem involvement and disease variability of myotonic dystrophy have presented challenges for clinical care and research.
openaire   +2 more sources