Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations.
Chikhaoui A, Kraoua I, Calmels N, Bouchoucha S, Obringer C, Zayoud K, Montagne B, M'rad R, Abdelhak S, Laugel V, Ricchetti M, Turki I, Yacoub-Youssef H.
Chikhaoui A, et al. Among authors: montagne b.
Orphanet J Rare Dis. 2022 Mar 5;17(1):121. doi: 10.1186/s13023-022-02257-1.
Orphanet J Rare Dis. 2022.
PMID: 35248096
Free PMC article.