CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability

Nouvelle publication de l’UMR8199 : CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability

https://www.molmetab.com/article/S2212-8778%2818%2930427-7/fulltext?rss=yes