Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing-Reference-Cited by-同舟云学术

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

Published:2016-03-22 Issue:1 Volume:11 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Calmels Nadège,Greff Géraldine,Obringer Cathy,Kempf Nadine,Gasnier Claire,Tarabeux Julien,Miguet Marguerite,Baujat Geneviève,Bessis Didier,Bretones Patricia,Cavau Anne,Digeon Béatrice,Doco-Fenzy Martine,Doray Bérénice,Feillet François,Gardeazabal Jesus,Gener Blanca,Julia Sophie,Llano-Rivas Isabel,Mazur Artur,Michot Caroline,Renaldo-Robin Florence,Rossi Massimiliano,Sabouraud Pascal,Keren Boris,Depienne Christel,Muller Jean,Mandel Jean-Louis,Laugel Vincent

Funder

Agence de la Biomédecine (FR)

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-016-0408-0

Reference74 articles.

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