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Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome
Mohammadi-asl, J., Hajjari, M., Tahmasebi Birgani, M., Riahi, K., Nasiri, H., Kollaee, A.Language:
english
Journal:
Annals of Human Genetics
DOI:
10.1111/ahg.12255
Date:
July, 2018
File:
PDF, 772 KB
english, 2018