TY  - JOUR
AU  - Moore, Ursula
AU  - Gordish, Heather
AU  - Diaz-Manera, Jordi
AU  - James, Meredith K
AU  - Mayhew, Anna G
AU  - Guglieri, Michela
AU  - Fernandez-Torron, Roberto
AU  - Rufibach, Laura E
AU  - Feng, Jia
AU  - Blamire, Andrew M
AU  - Carlier, Pierre G
AU  - Spuler, Simone
AU  - Day, John W
AU  - Jones, Kristi J
AU  - Bharucha-Goebel, Diana X
AU  - Salort-Campana, Emmanuelle
AU  - Pestronk, Alan
AU  - Walter, Maggie C
AU  - Paradas, Carmen
AU  - Stojkovic, Tanya
AU  - Mori-Yoshimura, Madoka
AU  - Bravver, Elena
AU  - Pegoraro, Elena
AU  - Lowes, Linda Pax
AU  - Mendell, Jerry R
AU  - Bushby, Kate
AU  - Straub, Volker
AU  - Jain COS Consortium
PY  - 2021
DO  - 10.1016/j.nmd.2021.01.009
UR  - http://hdl.handle.net/10668/17205
T2  - Neuromuscular disorders : NMD
AB  - This study aims to determine clinically relevant phenotypic differences between the two most common phenotypic classifications in dysferlinopathy, limb girdle muscular dystrophy R2 (LGMDR2) and Miyoshi myopathy (MMD1). LGMDR2 and MMD1 are reported to...
LA  - en
KW  - [16] Clinical neurology examination
KW  - [176] All neuromuscular disease
KW  - [185] Muscle disease
KW  - [21] Clinical trials methodology
KW  - [54] Cohort study
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Disease Progression
KW  - Distal Myopathies
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Muscle Weakness
KW  - Muscular Atrophy
KW  - Muscular Dystrophies, Limb-Girdle
KW  - Phenotype
KW  - Young Adult
TI  - Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease.
TY  - research article
VL  - 31
ER  -