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Deciphering the role of MYC Gene Variants in Childhood Cerebral Adrenoleukodystrophy (ccALD) using Integrative Transcriptomic and Variant Analysis

Objective: Childhood cerebral adrenoleukodystrophy (ccALD) is a severe neurodegenerative disorder characterized by rapid demyelination and disruption of the blood-brain barrier (BBB). Although mutations in the ABCD1 gene are the primary cause of the disease, the downstream molecular mechanisms contr...

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Bibliografiset tiedot
Päätekijät: Jain Chakresh Kumar, Maurya Sarita, Tripathi Pankaj Kumar, Mishra Divya
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: EDP Sciences 2026-01-01
Sarja:BIO Web of Conferences
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Linkit:https://www.bio-conferences.org/articles/bioconf/pdf/2026/26/bioconf_icabb2026_01017.pdf
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