A Roma founder <i>BIN1</i> mutation causes a novel phenotype of centronuclear myopathy with rigid spine
Macarena Cabrera‐Serrano(The University of Western Australia), Carmen Paradas(Instituto de Salud Carlos III)
Cited by 23
Related Papers
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss
|EMBO Molecular Medicine|2016|105
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy
|Neuromuscular Disorders|2011|96
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
|Nature Communications|2024|28