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

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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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An: 131218499
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  Data: Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.
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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Human+Genetics%22">Annals of Human Genetics</searchLink>. Sep2018, Vol. 82 Issue 5, p304-308. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=131218499
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        Value: 10.1111/ahg.12255
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      – Code: eng
        Text: English
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        PageCount: 5
        StartPage: 304
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      – TitleFull: Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome.
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            NameFull: Hajjari, M.
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            NameFull: Tahmasebi Birgani, M.
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            NameFull: Riahi, K.
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            NameFull: Nasiri, H.
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            – D: 01
              M: 09
              Text: Sep2018
              Type: published
              Y: 2018
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