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Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.

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Title: Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.
Authors: Calmels, Nadège1 nadege.calmels@chru-strasbourg.fr, Greff, Géraldine1, Obringer, Cathy2, Kempf, Nadine1, Gasnier, Claire1, Tarabeux, Julien1, Miguet, Marguerite1, Baujat, Geneviève3, Bessis, Didier4, Bretones, Patricia5, Cavau, Anne6, Digeon, Béatrice7, Doco-Fenzy, Martine8, Doray, Bérénice9, Feillet, François10, Gardeazabal, Jesus11, Gener, Blanca12, Julia, Sophie13, Llano-Rivas, Isabel12, Mazur, Artur14
Source: Orphanet Journal of Rare Diseases. 3/22/2016, Vol. 11, p1-16. 16p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 3/22/2016, Vol. 11, p1-16. 16p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=113988578
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              Text: 3/22/2016
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