C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis.
De Decker M, Zelina P, Moens TG, Beckers J, Contardo M, Dittlau KS, Van Schoor E, Ronisz A, Eggermont K, Moisse M, Chandran S, Veldink JH, Thal DR, Van Den Bosch L, Pasterkamp RJ, Van Damme P.
De Decker M, et al. Among authors: chandran s.
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Brain. 2024.
PMID: 39703094