Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing | Orphanet Journal of Rare Diseases | Full Text

Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing | Orphanet Journal of Rare Diseases | Full Text

The following new article has just been published in Orphanet Journal of Rare Diseases

Research  

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, Laugel V

Orphanet Journal of Rare Diseases 2016, 11 :26 (22 March 2016)

Abstract | Full Text | PDF