Associated Papers
Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy.
Tahmasebi-Birgani M et al.
Iranian Journal of Basic Medical Sciences, 2019
Novel hemizygous nonsense mutation in DRP2 is associated with inherited neuropathy.
Roda RH et al.
Neurology. Genetics, 2018
Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth disease.
Brennan KM et al.
Neuromuscular Disorders : Nmd, 2015
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