Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy

<h4>Introductions</h4> Duchenne muscular dystrophy (DMD) is an X-linked recessive progressive muscular disease marked by developmental delays due to mutations in the DMD gene, which encodes dystrophin. Brain comorbidity adds to the burden of limited mobility and significantly impacts pat...

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Hlavní autoři: Kristy Iskandar, Agung Triono, Sunartini, Ery Kus Dwianingsih, Braghmandita Widya Indraswari, Ignatia Rosalia Kirana, Gabriele Ivana, Retno Sutomo, Suryono Yudha Patria, Elisabeth Siti Herini, Gunadi
Médium: Článek
Jazyk:English
Vydáno: Public Library of Science (PLoS) 2022-01-01
Edice:PLoS ONE
On-line přístup:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621454/?tool=EBI