학술논문
Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing
Document Type
Article
Author
Calmels, N.; Greff, G.; Kempf, N.; Gasnier, C.; Tarabeux, J.; Miguet, M.; Muller, J.; Mandel, J.-L.; Obringer, C.; Laugel, V.; Baujat, G.; Bessis, D.; Bretones, P.; Cavau, A.; Digeon, B.; Doco-Fenzy, M.; Doray, B.; Feillet, F.; Gardeazabal, J.; Gener, B.; Llano-Rivas, I.; Julia, S.; Mazur, A.; Michot, C.; Renaldo-Robin, F.; Rossi, M.; Sabouraud, P.; Keren, B.; Depienne, C.
Source
In: Orphanet Journal of Rare Diseases . (Orphanet Journal of Rare Diseases, 2016, 11(1))
Subject
Language
English
ISSN
17501172