Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is a progressive degenerative illness that affects 1 in every 6 to 11,000 live births. This autosomal recessive disorder is caused by homozygous deletion or mutation of the SMN1 gene (survival motor neuron). As a backup, the SMN1 gene has the SMN2 gene, which produces o...

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Detalles Bibliográficos
Autores principales: Babić, Marija, Banović, Maria, Berečić, Ivana, Banić, Tea, Babić Leko, Mirjana, Ulamec, Monika, Junaković, Alisa, Kopić, Janja, Sertić, Jadranka, Barišić, Nina, Šimić, Goran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419842/
https://www.ncbi.nlm.nih.gov/pubmed/37568462
http://dx.doi.org/10.3390/jcm12155060

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