CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.
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Montagne L, et al. Among authors: lenne b.
Mol Metab. 2018 Jul;13:1-9. doi: 10.1016/j.molmet.2018.05.005. Epub 2018 May 16.
Mol Metab. 2018.
PMID: 29784605
Free PMC article.