Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.

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Bibliographic Details
Title: Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.
Authors: Mohammadi‐asl, J.1,2, Hajjari, M.3 Mohamad.hajari@gmail.com, Tahmasebi Birgani, M.1 maryam_tahmaseby@yahoo.com, Riahi, K.4,5, Nasiri, H.6, Kollaee, A.2
Source: Annals of Human Genetics. Sep2018, Vol. 82 Issue 5, p304-308. 5p.
Database: Academic Search Ultimate
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Description
ISSN:00034800
DOI:10.1111/ahg.12255