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Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations.

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Bibliographic Details
Title:	Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations.
Authors:	Chikhaoui, Asma¹ (AUTHOR), Kraoua, Ichraf^1,2 (AUTHOR), Calmels, Nadège^3,4 (AUTHOR), Bouchoucha, Sami^1,5 (AUTHOR), Obringer, Cathy⁴ (AUTHOR), Zayoud, Khouloud¹ (AUTHOR), Montagne, Benjamin⁶ (AUTHOR), M'rad, Ridha^7,8 (AUTHOR), Abdelhak, Sonia¹ (AUTHOR), Laugel, Vincent⁴ (AUTHOR), Ricchetti, Miria⁶ (AUTHOR), Turki, Ilhem² (AUTHOR), Yacoub-Youssef, Houda¹ (AUTHOR) houda.yacoub@pasteur.utm.tn
Source:	Orphanet Journal of Rare Diseases. 3/5/2022, Vol. 17 Issue 1, p1-14. 14p.
Database:	Academic Search Ultimate
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Description
ISSN:	17501172
DOI:	10.1186/s13023-022-02257-1