Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing
- Calmels, N.
- Greff, G.
- Obringer, C.
- Kempf, N.
- Gasnier, C.
- Tarabeux, J.
- Miguet, M.
- Baujat, G.
- Bessis, D.
- Bretones, P.
- Cavau, A.
- Digeon, B.
- Doco-Fenzy, M.
- Doray, B.
- Feillet, F.
- Gardeazabal, J.
- Gener, B.
- Julia, S.
- Llano-Rivas, I.
- Mazur, A.
- Michot, C.
- Renaldo-Robin, F.
- Rossi, M.
- Sabouraud, P.
- Keren, B.
- Depienne, C.
- Muller, J.
- Mandel, J.-L.
- Laugel, V.
- Montrer des auteurs +
Revue:
Orphanet Journal of Rare Diseases
ISSN: 1750-1172
Année de publication: 2016
Volumen: 11
Número: 1
Type: Article
