Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy

INTRODUCTIONS: 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 patients’ quality of li...

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Detalles Bibliográficos
Autores principales: Iskandar, Kristy, Triono, Agung, Sunartini, Dwianingsih, Ery Kus, Indraswari, Braghmandita Widya, Kirana, Ignatia Rosalia, Ivana, Gabriele, Sutomo, Retno, Patria, Suryono Yudha, Herini, Elisabeth Siti, Gunadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621454/
https://www.ncbi.nlm.nih.gov/pubmed/36315559
http://dx.doi.org/10.1371/journal.pone.0276640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621454/
https://www.ncbi.nlm.nih.gov/pubmed/36315559
http://dx.doi.org/10.1371/journal.pone.0276640

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