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First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene

Crossref DOI link: https://doi.org/10.1186/s12881-018-0677-7

Published Online: 2018-09-10

Published Print: 2018-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Chebly, Alain https://orcid.org/0000-0001-5582-2923
Corbani, Sandra

Abou Ghoch, Joelle

Mehawej, Cybel

Megarbane, André

Chouery, Eliane
Funding

Funding for this research was provided by:

Saint Joseph University
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Article History

Received: 3 May 2018

Accepted: 31 August 2018

First Online: 10 September 2018

Ethics approval and consent to participate

: This study was approved by the Ethical Committee of Saint Joseph University (USJ), Beirut, Lebanon. Peripheral blood samples were obtained from the three patients after obtaining written informed consent from the parents.

: Written consent has been obtained from the parents for publication of clinical details and biological data.

: EC is a member of the editorial board of this journal. The other authors declare they have no competing interests.

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